| Not Yet Recruiting | Lacrima VR for Dry Eye Disease and Meibomian Gland Dysfunction NCT07415330 | Demaod Ltd | N/A |
| Not Yet Recruiting | Blink Reminders and Meibomian Gland Loss in Digital Screen Users NCT07430137 | Asociación para Evitar la Ceguera en México | N/A |
| Not Yet Recruiting | Study to Evaluate the Safety and Tolerability of PRO-190 Ophthalmic Solution Compared to Systane Ultra® on the NCT06379685 | Laboratorios Sophia S.A de C.V. | Phase 1 |
| Not Yet Recruiting | Switching From Xiidra to TRYPTYR NCT07267481 | Southern College of Optometry | Phase 4 |
| Not Yet Recruiting | Study of Platelet Rich Plasma Drops to Moderate Clinically Significant Dry Eye NCT05121493 | University of Rochester | N/A |
| Not Yet Recruiting | Phase III Study of Topical Fibrinogen-Depleted Human Platelet Lysate Compared to Placebo for Moderate to Sever NCT06903611 | Cambium Bio Limited | Phase 3 |
| Recruiting | Clinical Investigation Between the Topical Administration of a Tear Substitute With Ancillary Medicinal Substa NCT07412860 | FB Vision S.p.A | N/A |
| Active Not Recruiting | The Impact of Hypothyroidism on Tear Production and Dry Eye Symptoms: Implications for Optometric Care NCT06913465 | Superior University | — |
| Active Not Recruiting | Comparison Of Blue Light Filter Feature and Blue Blocking Lenses in Digital Device Users With Dry Eye Patients NCT06913504 | Superior University | N/A |
| Recruiting | Efficacy of Platelet-Rich Plasma Injection in Dry Eye Syndrome NCT06831253 | Centre Hospitalier Universitaire de Nice | N/A |
| Completed | Laser Acupuncture for Dry Eye Disease Due to Visual Display Terminal Use NCT06688630 | Indonesia University | N/A |
| Recruiting | Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD NCT06220474 | The University of Hong Kong | N/A |
| Recruiting | Difference of Tear Ferning Between Women with and Without Menopausal. NCT06848829 | Chung Shan Medical University | N/A |
| Recruiting | Protecting the Eyes of Gamers With Lubricating Eyedrops NCT06163989 | Aston University | N/A |
| Not Yet Recruiting | iTear Single-center, Open-label, Single-arm Study NCT06525961 | The University of Hong Kong | Phase 4 |
| Recruiting | Limbal Stem Cell Derived Exosome (LSC-Exo) Eye Drop for Treatment of Dry Eye NCT06543667 | Iran University of Medical Sciences | Phase 1 |
| Completed | Traditional Chinese Medicine Ultrasonic Atomization Treatment for Dry Eye Disease NCT06089317 | Chinese University of Hong Kong | N/A |
| Completed | Preoperative iLux on Cataract Surgery Derived Dry Eye Disease Due to Meibomian Gland Dysfunction NCT06483750 | George Washington University | N/A |
| Completed | To Evaluate the Efficacy and Safety of HUC3-053 in Patients With Dry Eye Syndrome NCT06388070 | Huons Co., Ltd. | Phase 3 |
| Not Yet Recruiting | Assessment of Tear Production, Corneal Staining, and Comfort Level Wearing Different Types of Contact Lenses NCT06351410 | National University of Malaysia | N/A |
| Recruiting | Photobiomodulation With REd vs BluE Light (REBEL) NCT06371300 | Aston University | N/A |
| Completed | Tear Ferning Test for Dry Eye Diagnosis NCT06364943 | Chung Shan Medical University | N/A |
| Unknown | Evaluation of Dry Eye Disease's Signs in Patients Who Were Administered Intravitreal Anti-VEGF Injections NCT06317922 | Francesco Bandello | N/A |
| Unknown | Dual-Polymer Hydroxypropyl Guar-and Hyaluronic Acid Lubricants in Rheumatoid Arthritis NCT06209879 | Chang Gung Memorial Hospital | Phase 4 |
| Unknown | BroadBand Light for the Treatment of Dry Eye Disease NCT06174064 | University of Southern California | N/A |
| Completed | Efficacy of a New Nanoemulsion Artificial Tear Targeting Dry Eye Disease NCT06188260 | The Hong Kong Polytechnic University | Phase 2 |
| Completed | Lubricating Effectiveness of Carragelose Eye Drops in Patients Affected by Mild to Moderate Dry Eye NCT06262100 | Marinomed Biotech AG | N/A |
| Active Not Recruiting | A Comparative Study Between Preservative With Benzalkonium Chloride vs Preservative Free Eye Drops on the Ocul NCT06404541 | Kasr El Aini Hospital | Phase 4 |
| Recruiting | Efficacy and Safety of AJU-S56 5% in Dry Eye Syndrome Patients NCT06291194 | AJU Pharm Co., Ltd. | Phase 3 |
| Completed | Mechanisms of Light-based Therapies for Dry Eye Disease NCT06004895 | Aston University | N/A |
| Terminated | A Study to Assess the Safety and Efficacy of IC265 Ophthalmic Solution for Dry Eye in Adult Participants NCT05992922 | Iacta Pharmaceuticals | Phase 2 |
| Completed | Preventive TREatment of Dry Eye in Patients Receiving Repeated Intravitreal Injections for Age-related Macular NCT06174181 | Direction Centrale du Service de Santé des Armées | N/A |
| Active Not Recruiting | Therapeutic Effect of Stem Cell Eye Drops on Dry Eye Disease NCT05784519 | The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School | EARLY_Phase 1 |
| Unknown | The Effect of a Pre-cataract Surgical Ocular Hygiene Regime on Microbial Load, Tear Osmolarity, Dry Eye, and I NCT05990712 | Uptown Eye Specialists | Phase 4 |
| Completed | Feasibility of Dynamic Muscle Stimulation + Radiofrequency for Improving Blink Quality in Subjects with Dry Ey NCT05945069 | Lumenis Be Ltd. | N/A |
| Completed | Comparing Efficacy and Safety of TJO-083 in Dry Eye Diseases Patients NCT06427031 | Taejoon Pharmaceutical Co., Ltd. | Phase 3 |
| Recruiting | Salivary Conductivity Screening for Dry Eye Disease and Sjögren's Syndrome NCT06406933 | Chang Gung Memorial Hospital | — |
| Completed | Efficacy and Safety Evaluation of Tavilermide Ophthalmic Solution for the Treatment of Dry Eye NCT05848128 | Mimetogen Pharmaceuticals USA, Inc. | Phase 3 |
| Unknown | Evaluation of Optical System in the Treatment of - Dry Eye Disease NCT05741398 | Demaod Ltd | N/A |
| Completed | Intra-Nasal Mechanical Stimulation (INMEST) As a Treatment Method for the Relief of Symptoms of Dry Eye NCT05887336 | Abilion Medical Systems AB | N/A |
| Completed | OTX-DED for the Short-term Treatment of the Symptoms of Dry Eye Disease (DED) NCT05814757 | Ocular Therapeutix, Inc. | Phase 2 |
| Unknown | Omega-3 Fatty Acid Supplementation and Tear Film Quality in Celiac Patients NCT05825976 | Josip Juraj Strossmayer University of Osijek | N/A |
| Completed | Investigation of Preservative-Free Ophthalmic Solution in Ocular Dryness NCT05778942 | SIFI SpA | — |
| Completed | A Feasibility Study to Evaluate the Tolerability of Oph1 Compared to Restasis in Healthy Volunteers NCT05184517 | OphRx Ltd. | EARLY_Phase 1 |
| Completed | Clinical Trial to Evaluate the Safety and Efficacy of SCAI-001 Compared to Restasis NCT05733624 | SCAI Therapeutics | Phase 2 |
| Suspended | Prospective Study to Validate the Imaging Biomarker for NCP (R33) NCT05653921 | Tufts Medical Center | — |
| Completed | Lifitegrast Eye Drops in Healthy Subjects:Phase I Study NCT07040826 | Qilu Pharmaceutical Co., Ltd. | Phase 1 |
| Completed | Effect of Micropulse Laser on Dry Eye Disease Due to Meibomian Gland Dysfunction NCT04425551 | Naval Hospital, Athens | N/A |
| Unknown | Prevalence of Different Etiologies of Ocular Dryness in Patients Previously Diagnosed With Dry Eye Disease in NCT05598437 | Roweis adel youssef | — |
| Completed | to Evaluate the Effectiveness and Safety of the Tixel® , VS LipiFlow® in the Treatment of Meibomian Gland Dysf NCT05162261 | Novoxel Ltd. | N/A |
| Completed | Efficacy and Safety Safety of Nutritears® in Adults With Dry Eye Syndrome NCT05481450 | Applied Science & Performance Institute | N/A |
| Active Not Recruiting | Efficacy of OmegaBoost to Increase Omega-3 Levels in Healthy Individuals NCT05763940 | Western University of Health Sciences | N/A |
| Unknown | Effect of Exercises on Computer Vision Syndrome NCT05414799 | Shifa Tameer-e-Millat University | N/A |
| Completed | Effects of Carboxymethylcellulose Artificial Tears on the Eye Microbiome NCT05292755 | University of Florida | Phase 4 |
| Completed | A Clinical Trial to Evaluate the Safety and Efficacy of Rreproxalap in Adults With Dry Eye Disease NCT05424549 | Aldeyra Therapeutics, Inc. | Phase 2 |
| Unknown | A Usability Study of External Neuromodulation With iTEAR100 Generation 2 NCT05304650 | Olympic Ophthalmics, Inc. | Phase 4 |
| Completed | A Phase 3, Multi-Center Study Evaluating PL9643 in Patients with Dry Eye NCT05201170 | Palatin Technologies, Inc | Phase 3 |
| Completed | Efficacy and Safety of AJU-S56 in Dry Eye Syndrome Patients NCT06337981 | AJU Pharm Co., Ltd. | Phase 2 |
| Completed | Optimization of the Ocular Surface Prior to Cataract Surgery Using PROKERA NCT05148507 | Jeff Wongskhaluang | N/A |
| Unknown | Effect of Topical Antioxidants in Dry Eye Disease and Diabetic Retinopathy NCT05429229 | Adolfo Daniel Rodriguez-Carrizalez | Phase 2 |
| Completed | Impact of Vitamin D3 Supplementation in Non-Sjogren Dry Eye Patients With Low Serum Vitamin D Level NCT05425914 | University of Faisalabad | Phase 3 |
| Completed | Evaluate the Safety and Effectiveness of The Tixel Fractional System in the Treatment of Meibomian Gland Disfu NCT04889950 | Novoxel Ltd. | N/A |
| Unknown | The Proportion of Patients Diagnosed With Dry Eye by the Asia Dry Eye Society (ADES) Criteria in Taiwan (DECS- NCT05096546 | Far Eastern Memorial Hospital | — |
| Unknown | Comparing Efficacy and Safety of TJO-083 in Dry Eye Disease Patients NCT05346783 | Taejoon Pharmaceutical Co., Ltd. | Phase 1 / Phase 2 |
| Completed | 3 Month Study of Cationorm Pro Versus Vismed in Adults With Dry Eye Disease Related to Keratitis or Keratoconj NCT04701086 | Santen SAS | N/A |
| Completed | Computer Screen Properties Study NCT05042960 | NYU Langone Health | N/A |
| Completed | CEQUA for Sjogren's Syndrome Dry Eye NCT04835623 | Center for Ophthalmic and Vision Research, LLC | Phase 4 |
| Active Not Recruiting | 3 Month Study of Alocross Versus Vismed in Adults With Dry Eye Disease Related to Keratitis or Keratoconjuncti NCT04685109 | Santen SAS | N/A |
| Unknown | Evaluation Of Vision Recovery And Comfort Index In Patients With Borderline/Mild Dry Eyes Undergoing FLACS Wit NCT04863742 | Sight Medical Doctors PLLC | Phase 4 |
| Unknown | Phase 2 Clinical Trial to Evaluate the Efficacy and Safety of GLH8NDE in Patients With Dry Eye Disease NCT04679883 | GL Pharm Tech Corporation | Phase 2 |
| Unknown | Effect of Traditional Chinese Medicine on Basic Tear Secretion and Tear Cytokines in Patients With Dry Eye Dis NCT04785261 | China Medical University Hospital | Phase 2 |
| Completed | Treatment Regimens in Meibomian Gland Dysfunction NCT05594745 | Tauber Eye Center | Phase 4 |
| Withdrawn | Effect of Lifitegrast 5% on Tear Film Markers NCT03952481 | Weill Medical College of Cornell University | Phase 4 |
| Unknown | Quantum Molecular Resonance Effects on Patients With Dry Eye Disease NCT05469932 | Assaf-Harofeh Medical Center | N/A |
| Completed | Management of Dry Eye Disease After Cataract Surgery With Topical Hyaluronic Acid and Gingko Biloba NCT05002036 | University of Milan | Phase 4 |
| Unknown | The Effect of 3% Diquafosol Ophthalmic Solution on Visual Display Terminal-associated Dry Eye NCT04668118 | Peking University Third Hospital | Phase 4 |
| Unknown | Mask-associated Dry Eye Symptoms in China NCT04744805 | Tianjin Eye Hospital | — |
| Completed | Differential Diagnosis of Sjögren's Versus Non-Sjögren's Dry Eye NCT04493658 | Johns Hopkins University | — |
| Unknown | Platelet Rich Plasma Eye Drops for Treatment of Ocular Surface Disease NCT04608084 | University Health Network, Toronto | Phase 4 |
| Completed | Pilot Study to Investigate the Feasibility, Reliability and Efficacy of Utilizing OCT to Automate PROSE Fittin NCT04649177 | Boston Sight | N/A |
| Completed | The TRANQUILITY Trial: Clinical Trial to Assess the Efficacy and Safety in Subjects With Dry Eye Disease NCT04674358 | Aldeyra Therapeutics, Inc. | Phase 2 / Phase 3 |
| Completed | Topical Naloxone to Diagnose Ocular Pain NCT04454281 | Seema Capoor | Phase 1 |
| Completed | Effect of Ciclosporin Eyedrops on Sjögren Syndrome NCT04597762 | Hospital Hietzing | N/A |
| Completed | The Effect of Cyclosporin Before Cataract Surgery NCT04426240 | Samsung Medical Center | Phase 4 |
| Unknown | Metabolomic Profile in Dry Eye Syndrome Patients. NCT05433428 | Ifocus Oyeklinikk | Phase 4 |
| Terminated | Xiidra vs. Xiidra + Dextenza Treatment for Dry Eye Disease NCT04413253 | Eye Surgeons of Indiana | Phase 4 |
| Completed | Lipiflow Treatment Alone vs. Lipiflow + Dextenza Treatment for Dry Eye Disease NCT04413279 | Eye Surgeons of Indiana | Phase 4 |
| Unknown | CDSS of Traditional Chinese Medicine Intervention for Dry Eye Syndrome NCT04806256 | Peking University Third Hospital | N/A |
| Unknown | Clinical Investigation to Assess the Efficacy and the Safety of VisuXL® Gel Administered in Patients Affected NCT04485533 | VISUfarma SpA | N/A |
| Completed | Effect of Cequa Treatment on Accuracy of Pre-operative Biometry & Higher Order Aberrations in Dry Eye Patients NCT04342988 | Research Insight LLC | Phase 4 |
| Completed | Clinical Effect of MiboFlo in Dry Eye Patients NCT04310969 | Beijing Tongren Hospital | N/A |
| Withdrawn | Clinical Efficacy of Intense Pulsed Light(IPL) Procedure in Dry Eye Patient NCT04391907 | Samsung Medical Center | N/A |
| Completed | [KSR-001-P02] Phase 2b/3 Study, Evaluate the Efficacy and Safety of KSR-001 in Patients With Dry Eye Syndrome NCT05017844 | Kukje Pharma | Phase 2 / Phase 3 |
| Completed | Efficacy and Safety of Ikervis Under Controlled Environmental Conditions Environment NCT04492878 | Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA | Phase 4 |
| Completed | Differences in Dry Eye Symptoms Related to Geographic Location in Spain and Impact of Artificial Tears Use NCT06499753 | University of Valladolid | — |
| Terminated | Prospective Study To Assess The Safety And Effectiveness Of Tixel Treatment On Dry Eye Symptoms In Asian Patie NCT04260893 | Novoxel Ltd. | N/A |
| Unknown | Umbilical Cord Serum Versus Conventional Eyedrops NCT04217785 | National University of Malaysia | Phase 1 / Phase 2 |
| Completed | ACCURATE Study for Subjects With Dry Eyes NCT04237012 | The Eye Centers of Racine and Kenosha | Phase 4 |
| Completed | Evaluating HA 0.15% Compared With Cyclosporine 0.05%, and Efficacy of Combination Therapy in Dry Eye Disease P NCT04127851 | Taejoon Pharmaceutical Co., Ltd. | Phase 4 |
| Terminated | Viveye Ocular Magnetic Neurostimulation System (OMNS) for the Management of Severe Dry Eye Disease NCT04143841 | Epitech Mag Ltd. | N/A |
| Completed | Intense Pulsed Light in Meibomian Gland Dysfunctions NCT04147962 | Centre Hospitalier Universitaire de Saint Etienne | — |
| Completed | A Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristics of GLH8NDE After Sin NCT04104997 | GL Pharm Tech Corporation | Phase 1 |
| Completed | An Open-Label, Multi-Center, Clinical Study Evaluating the Effect of the NDE L68 StableFit® Punctal Plug on th NCT04280653 | Mati Therapeutics Inc. | N/A |
| Completed | Effect of Intraoperative Dexamethasone on Post-op Dry Eye NCT04184999 | SR Cornea Consultants | Phase 4 |
| Completed | Assessing the Impact of Tixel Treatment of Periorbital Wrinkles on Dry Eye Symptoms and Signs NCT04730336 | Aston University | N/A |
| Completed | A Non-inferiority Study of Eyestil® Plus Multidose Versus Vismed Multi® NCT03803748 | SIFI SpA | N/A |
| Unknown | The Effect of Combination of Vitamin A, Vitamin E, Sodium Hyaluronate 0.15% Eye Drop Compared With Sodium Hyal NCT04000789 | Dr Cipto Mangunkusumo General Hospital | N/A |
| Terminated | Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in Dry Eye Disease NCT03827564 | Allergan | N/A |
| Completed | Meibomian Gland Dysfunction Management With ZEST Protocol NCT03968731 | University of the Incarnate Word | N/A |
| Completed | The Effect of Punctal Plugs on Ocular Surface After Povidone-Iodine Preparation of Intravitreal Injection NCT03945071 | University of Oklahoma | N/A |
| Completed | Quality of Life and Visual Acuity of Visglyc Eye Drops on Dry Eye Patients NCT04063644 | OPKO Health, Inc. | N/A |
| Completed | Assessment of the Safety and Efficacy of RGN-259 Ophthalmic Solutions for Dry Eye Syndrome: ARISE-3 NCT03937882 | ReGenTree, LLC | Phase 3 |
| Completed | HU007 Eye Drops in Patients With Dry Eye Syndrome NCT04384991 | Huons Co., Ltd. | Phase 3 |
| Completed | Efficacy of T2259 in DED NCT03874429 | Laboratoires Thea | N/A |
| Completed | Pharmacokinetics, Safety, and Tolerability of rhEGF Eye Drops in Healthy Male Subjects NCT05219461 | Daewoong Bio Inc. | Phase 1 |
| Completed | Amniotic Membrane Treatment for Hyposecretory Dry Eye NCT05598242 | Hospital Nacional Profesor Alejandro Posadas | Phase 3 |
| Completed | Corneal Epithelial Stem Cells and Dry Eye Disease NCT03302273 | Sloan W. Rush, MD | N/A |
| Completed | Effects of RP101 in Post-menopausal Women With Dry Eye Syndrome NCT03821415 | Redwood Pharma AB | Phase 2 |
| Completed | Pilot Study of TearCare System - Long-Term Extension NCT03804502 | Sight Sciences, Inc. | N/A |
| Completed | Tear Lipid Layer Thickness Changes With Use of Emollient and Non-Emollient Eye Drops NCT03706443 | Ohio State University | N/A |
| Completed | [KSR-001-P01]Clinical Trial to Evaluate the Safety, Tolerability and Pharmacokinetic Characteristic of KSR-001 NCT05017870 | Kukje Pharma | Phase 1 |
| Completed | TrueTear in Sjogren's Disease Patients NCT03719885 | University of Pennsylvania | N/A |
| Completed | Efficiency and Changes of Cytokines Expression in Tear After Intense Pulsed Light Treating Dry Eye Disease NCT04165785 | First Affiliated Hospital of Harbin Medical University | N/A |
| Completed | Safety and Tolerability of the Ophthalmic Gel PRO-165 Versus Artelac® Nightime Gel NCT03697876 | Laboratorios Sophia S.A de C.V. | Phase 1 |
| Completed | A Study to Assess the Safety and Effectiveness of SJP-0035 for the Treatment of Patients With Dry Eye Disease NCT03527212 | Senju Pharmaceutical Co., Ltd. | Phase 3 |
| Completed | Effect of ADDE on Tear Interferometry NCT05456061 | Yonsei University | N/A |
| Terminated | Management of Signs and Symptoms Associated With Dry Eye Disease NCT04015219 | BioTissue Holdings, Inc | N/A |
| Completed | Effectiveness and Safety of Intense Pulsed Light in Patients With Meibomian Gland Dysfunction NCT03518398 | Chulalongkorn University | Phase 3 |
| Terminated | Randomized Study of the Safety and Effectiveness of the TearCare System for the Signs and Symptoms of Dry Eye NCT03502447 | Sight Sciences, Inc. | N/A |
| Completed | Evaluation of an Updated Version of the Program "BlinkBlink" for Alleviation of Dry Eye Symptoms Induced by Co NCT04637516 | University of Applied Sciences and Arts Northwestern Switzerland | N/A |
| Unknown | Fingerprick Autologous Blood (FAB) in Severe Dry Eye Disease (DED) NCT03395431 | Bedford Hospital NHS Trust | N/A |
| Completed | Tangible Hydra-PEG: A Promising Solution for Scleral Lens Wearers With Dry Eye NCT03417505 | Tangible Science | N/A |
| Unknown | Wumeiwan Jiawei Fang Use in Patients With Blepharospasm NCT05618470 | China Academy of Chinese Medical Sciences | Phase 2 / Phase 3 |
| Completed | Effect of Topical Azithromycin on Tear Film Thickness in Patients With Meibomian Gland Dysfunction NCT03162497 | Medical University of Vienna | Phase 4 |
| Unknown | Diadenosine Polyphosphates and Mucin Associated With Ocular Surface Disorders NCT03731624 | Taipei Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation | — |
| Recruiting | Three-dimensional Analysis of EMMPRIN on Conjunctival Epithelial Cells Surface in Severe Dry Eye Syndrome (ALT NCT03358979 | Fondation Ophtalmologique Adolphe de Rothschild | — |
| Completed | Clinical Study to Investigate the Efficacy and Safety of SJP002 Ophthalmic Solution in Patients With Dry Eye S NCT03723811 | Samjin Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Clinical Trial to Evaluate the Symptoms in Symptomatic Contact Lens Wearers Following Application of Intranasa NCT03325673 | Allergan | N/A |
| Completed | Pilot Study for Testing Safety of Repetitive Magnetic Stimulation for Treatment of Dry Eye NCT03012698 | Epitech Mag Ltd. | N/A |
| Completed | Optimization of the Treatment of Dry Eye Disease Caused by Meibomian Gland Dysfunction NCT03318874 | Oslo University Hospital | Phase 4 |
| Terminated | Clinical Study to Evaluate Tear Characteristics Following Acute TrueTear™ Use NCT03274999 | Allergan | N/A |
| Unknown | LAMELLEYE for the Treatment of Dry Eye Symptoms in pSS Patients NCT03140111 | NHS Greater Glasgow and Clyde | N/A |
| Completed | Crosslinked Hyaluronic Acid With Liposomes and Crocin in Dry Eye NCT03617315 | University of Seville | N/A |
| Recruiting | Assessment of TFT by OCT in Healthy Subjects and Subjects With DES NCT02585414 | Medical University of Vienna | — |
| Withdrawn | Punctal Plugs and Iodine Related Discomfort NCT03396809 | University of New Mexico | N/A |
| Completed | Safety and Efficacy of TrueTear™ for the Treatment of Meibomian Gland Disease NCT03226769 | Allergan | N/A |
| Completed | Safety and Tolerability of PRO-087 Versus Xyel Ofteno® and Systane Ultra®, on the Ocular Surface of Healthy Su NCT03524157 | Laboratorios Sophia S.A de C.V. | Phase 1 |
| Unknown | Ocular Micro-vascular Research Base on Functional Slip Lamp Biomicroscopy NCT03747614 | Zhongshan Ophthalmic Center, Sun Yat-sen University | Phase 4 |
| Completed | A Randomized, Double Masked, Clinical Study of Subjects With Dry Eye Syndrome NCT03162783 | Aldeyra Therapeutics, Inc. | Phase 2 |
| Terminated | Patients With Ocular Neuropathic Pain: Description of Pain and Impact on Their Quality of Life NCT03296111 | Fondation Ophtalmologique Adolphe de Rothschild | — |
| Completed | Effect of Lipid Based Eye Drops on Tear Film Lipid Layer Thickness NCT03399292 | Medical University of Vienna | — |
| Completed | Dry Eye Symptom Relief Assessment With Use of TrueTear in a Controlled Adverse Environment NCT03097614 | Oculeve, Inc. | N/A |
| Completed | Tear Lipid Layer Thickness With Emollient Eye Drops NCT03380624 | Ohio State University | Phase 4 |
| Completed | Lamelleye vs Comparator for the Treatment of Dry Eye Disease NCT03052140 | Glasgow Caledonian University | N/A |
| Completed | Effect of Single Instillation of Three Different Topical Lubricants on Tear Film Thickness in Patients With Dr NCT03161080 | Medical University of Vienna | N/A |
| Completed | Comparison Between Rebamipide 2% Versus Autologous Serum NCT03608761 | Hospital Nacional Profesor Alejandro Posadas | Phase 4 |
| Terminated | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye NCT02965846 | Allergan | Phase 3 |
| Completed | Topical Omega-3 Fatty Acids (REMOGEN® OMEGA) in the Treatment of Dry Eye NCT02908282 | TRB Chemedica AG | N/A |
| Completed | Evaluation of Dry Eye Symptoms in CAE With Application of Intranasal Neurostimulation NCT02910713 | Allergan | N/A |
| Terminated | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye NCT02815293 | Allergan | Phase 3 |
| Completed | A Two Comparator, Controlled Phase 3 Study in Patients With and Without Evaporative Dry Eye NCT02871440 | The University of New South Wales | Phase 3 |
| Completed | Tear Production by Nasal Neurostimulation Compared to Active Control NCT02970799 | Oculeve, Inc. | N/A |
| Unknown | Assessment of the Efficacy of Ocular Dipyridamole in the Treatment of Dry Eye Symptomology in Subjects With Pt NCT02782260 | Ariel University | Phase 2 |
| Completed | Safety and Efficacy of KPI-121 Compared to Placebo in Subjects With Dry Eye Disease NCT02819284 | Kala Pharmaceuticals, Inc. | Phase 3 |
| Completed | Safety and Efficacy of KPI-121 in Subjects With Dry Eye Disease NCT02813265 | Kala Pharmaceuticals, Inc. | Phase 3 |
| Unknown | Effect of Nursing Care on Prevention of Dry Eye NCT02767258 | Diego Dias de Araújo | N/A |
| Completed | Effects of a Moisturizing Product on Dry Eye and Skin NCT02683382 | Petra Larmo | N/A |
| Completed | Influence of Three Different Formulations of Lachrymal Substitutes on Tear Film Thickness and Other Signs and NCT02986750 | Medical University of Vienna | Phase 4 |
| Completed | Difference in the Frequency of Use of Lachrymal Substitutes in Patients With Moderate to Severe Dry Eye Syndro NCT02980913 | Medical University of Vienna | N/A |
| Completed | Added Benefits of Lachrymal Substitute Gel During the Night in Patients With Moderate to Severe Dry Eye Syndro NCT02585648 | Medical University of Vienna | N/A |
| Completed | A Safety and Efficacy Study of a New Eye Drop Formulation in Patients With Dry Eye Disease. NCT02553772 | Allergan | Phase 3 |
| Completed | CyclASol for the Treatment of Moderate to Severe Dry-eye Disease (DED) NCT02617667 | Novaliq GmbH | Phase 2 |
| Completed | Comparative Study of Rohto Dry-Aid® and Systane® Ultra in Patients With Dry Eye NCT03183089 | The Mentholatum Company | Phase 4 |
| Completed | Feasibility of IPL for Reducing Dry Eye Symptoms Caused by MGD NCT02621593 | Lumenis Be Ltd. | N/A |
| Unknown | 0.3% Sodium Hyaluronate in the Treatment of Dry Eye of Diabetic Patients NCT02595606 | Sun Yat-sen University | Phase 4 |
| Completed | Six Month Study to Evaluate the Safety and Effectiveness of the Intranasal Lacrimal Neurostimulator NCT02526290 | Oculeve, Inc. | N/A |
| Unknown | Effect of Benzalkonium Chloride Containing Eye Drops on the Conjunctival Bacterial Flora of Dry Eye Patients NCT02533154 | Medical University of Vienna | Phase 4 |
| Completed | Evaluation of Maintaining Visual Performance in Participants Who Engage in Electronic Visual Tasking While Usi NCT02554981 | Allergan | Phase 4 |
| Completed | Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Suspension in Patients With Dry E NCT02435914 | Allergan | Phase 2 |
| Completed | Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Participants and Participants With NCT02420730 | Allergan | Phase 1 |
| Completed | Multicenter Trial Evaluating Quality of Tears Produced by Nasal Neurostimulation NCT02385292 | Oculeve, Inc. | N/A |
| Completed | Influence of Lachrymal Substitute Gels on Tear Film Thickness in Patients With Moderate to Severe Dry Eye Synd NCT02585453 | Medical University of Vienna | Phase 4 |
| Completed | The Effect of Oral Zanthoxylum Schinifolium Seed Oil in Individuals With Dry Eye Disease NCT02802150 | Chonbuk National University Hospital | N/A |
| Completed | NovaTears® Eye Drops Observational Study NT-003 NCT02356328 | Novaliq GmbH | — |
| Completed | NovaTears® Eye Drops Observational Study NT-002 NCT02356341 | Novaliq GmbH | — |
| Completed | A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Genteal® Lubricant Gel Drops for Mod NCT02455050 | Allergan | Phase 3 |
| Completed | Evaluation of the Safety and Effectiveness of the Oculeve Intranasal Lacrimal Neurostimulator in Patients With NCT02313454 | Allergan | N/A |
| Completed | A Safety and Efficacy Study of Refresh Optive® Gel Drops in Patients With Dry Eye Disease NCT02280473 | Allergan | Phase 3 |
| Completed | Interest of Eye Movement Measurements in the Comprehension of Dry Eyes Symptoms NCT02851654 | Fondation Ophtalmologique Adolphe de Rothschild | — |
| Completed | A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye. NCT02205840 | Seikagaku Corporation | Phase 2 / Phase 3 |
| Completed | The Effect of Tear Supplements on Contact Lens Comfort NCT02956083 | University of the Incarnate Word | N/A |
| Completed | Safety and Efficacy of KPI-121 in Subjects With Dry Eye Disease NCT02188160 | Kala Pharmaceuticals, Inc. | Phase 2 |
| Completed | A Safety and Efficacy Study of OPTIVE FUSION™ With VISMED® Multi for the Management of Dry Eye NCT02117687 | Allergan | Phase 4 |
| Terminated | Phase 2 Study of a New Ophthalmic Formulation of Cyclosporine (Restasis® X) in Patients With Dry Eye Disease NCT02013791 | Allergan | Phase 2 |
| Completed | Investigation of Maintaining Visual Performance Achieved With Cyclosporine Therapy NCT02121847 | Allergan | Phase 4 |
| Unknown | Estrogen and the Outer Eye in Women During Fertility Treatment NCT02072122 | Meir Medical Center | — |
| Terminated | Effects of Sustained Reading on the Ocular Surface NCT02031172 | University of Rochester | — |
| Completed | Clinical Effects and Safety of 3% Diquafosol After Cataract Surgery NCT02608489 | Soonchunhyang University Hospital | N/A |
| Completed | Efficacy and Safety Study of TJCS for Treatment of Moderate to Severe Dry Eye Syndromes NCT02461719 | Taejoon Pharmaceutical Co., Ltd. | Phase 3 |
| Completed | A Study to Determine the Relief of Dry Eye Symptoms With the Use of TheraTears® Products (DUNLIN) NCT02014922 | University of Waterloo | Phase 4 |
| Completed | Study of Tisporin Eye Drops Group and Restasis Eye Drops Group After Treatment, Each Treatment Group Compariso NCT02229955 | Hanlim Pharm. Co., Ltd. | Phase 3 |
| Completed | A Safety and Efficacy Study of MIM-D3 Ophthalmic Solution for the Treatment of Dry Eye NCT01960010 | Mimetogen Pharmaceuticals USA, Inc. | Phase 3 |
| Completed | Ocular Surface Microbiome NCT02298881 | University of Washington | — |
| Completed | A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients Prior to Cataract Removal NCT01882413 | Allergan | — |
| Completed | An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy NCT01854905 | Allergan | — |
| Completed | Paralysis of the Orbicularis Muscle of the Eye in the Treatment for Dry Eye NCT02403219 | Instituto de Oftalmología Fundación Conde de Valenciana | Phase 1 |
| Completed | Impairment of Reading Ability in Dry Eye Patients NCT01826812 | Johns Hopkins University | — |
| Completed | A Pilot Study on the Use of a Sensory Panel to Assess Comfort Between Three Different Contact Lenses NCT01840787 | University of Waterloo | N/A |
| Completed | A Randomized, Parallel-Group Comparison Study of Topical Corticosteroids in Dry Eye Patients With Sjögren Synd NCT02011776 | Santen Pharmaceutical(China) Co.,LTD | — |
| Completed | Efficacy and Safety Study of Haporine-S for Treatment of Moderate to Severe Dry Eye Syndromes NCT01804361 | DH Bio Co., Ltd. | Phase 3 |
| Completed | Prevalence of Dry Eye Disease in Patients Diagnosed With Rheumatoid Arthritis NCT02252744 | Western University of Health Sciences | — |
| Completed | An Observational Study of OPTIVE PLUS® for the Treatment of Dry Eye Disease NCT01711424 | Allergan | — |
| Completed | Study of Cyclosporine Ophthalmic Soution Group and Cyclosporine Ophthalmic Suspension Group NCT01768312 | Hanlim Pharm. Co., Ltd. | Phase 3 |
| Completed | Non Interventional Study to Evaluate the Efficacy and Tolerability of Ectoin Containing Ophthalmic Solution NCT01684852 | Bitop AG | — |
| Completed | Comparison of the Efficacy and Safety of T2750 and Vismed® in the Treatment of Moderate to Severe Dry Eye Synd NCT01568593 | Laboratoires Thea | Phase 3 |
| Completed | A Clinical Study Evaluating the Safety and Efficacy of SI-614 Ophthalmic Solution in Patients With Dry Eye NCT01558999 | Seikagaku Corporation | Phase 2 |
| Completed | Safety Study of OPC-12759 Ophthalmic Solution NCT01471093 | Otsuka Pharmaceutical Co., Ltd. | Phase 1 |
| Completed | Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease NCT01459588 | Allergan | Phase 3 |
| Withdrawn | Treatment of Dry Eye With Supplements NCT01364311 | Medical University of Vienna | N/A |
| Completed | A Study of Sodium Carboxymethylcellulose for Post Cataract Surgery Dry Eye Symptoms NCT02028754 | Allergan | Phase 4 |
| Completed | Repeatability and Agreement of Anterior Segment Optical Coherence Tomography (AS-OCT) and Thermography NCT01479790 | Singapore National Eye Centre | N/A |
| Completed | Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in Patients With Dry Eye Disease NCT01294384 | Allergan | Phase 3 |
| Completed | Safety Evaluation of a New Preservative in a Lubricating Eye Drop NCT01434277 | Johnson & Johnson Consumer and Personal Products Worldwide | N/A |
| Unknown | Altaire Gel Forming Solution Versus Refresh Tears for the Treatment of Dry Eye Signs and Symptoms NCT01382810 | Innovative Medical | Phase 4 |
| Completed | The Effects of BAK on the Blood Aqueous Barrier of Pseudophakic Patients NCT01280110 | University of Campinas, Brazil | Phase 4 |
| Completed | Local Tolerability of Chitosan-N-acetylcysteine Eye Drops in Healthy Young Volunteers NCT01278784 | Medical University of Vienna | Phase 1 |
| Completed | Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunteers and in Patients With Dry E NCT01319773 | Allergan | Phase 1 |
| Completed | Evaluation of Screening Methods for Treatment of Meibomian Gland Dysfunction NCT01202747 | TearScience, Inc. | Phase 2 / Phase 3 |
| Completed | Safety and Tolerability of Chitosan-N-acetylcysteine Eye Drops in Healthy Young Volunteers NCT01015209 | Medical University of Vienna | Phase 1 |
| Completed | A Phase II, Dose Ranging Study Of CP-690,550 Eye Drops In Patients With Dry Eye Disease NCT01135511 | Pfizer | Phase 2 |
| Completed | TearLab Refractive Surgery Dry Eye Study NCT01176045 | TearLab Corporation | — |
| Completed | Dry Eye Assessment and Management: Feasibility Study NCT01102257 | Asbell, Penny, M.D. | Phase 2 / Phase 3 |
| Completed | Safety and Efficacy Study of Rebamipide 2% Ophthalmic Suspension in Patients With Dry Eye NCT01027013 | Kubota Vision Inc. | Phase 2 |
| Completed | Safety and Efficacy of Carboxymethylcellulose for Ocular Surface Integrity in Symptomatic Dry Eye NCT00987727 | Allergan | Phase 4 |
| Completed | Acupuncture for Dry Eye Syndrome NCT00969280 | Korea Institute of Oriental Medicine | Phase 3 |
| Completed | Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears for the Treatment of Dry Eye Si NCT00938704 | Allergan | Phase 4 |
| Completed | Confirmatory Study of OPC-12759 Ophthalmic Suspension NCT00885079 | Otsuka Pharmaceutical Co., Ltd. | Phase 3 |
| Completed | The Effect of Ocular Lubricant Eyedrops on Lid Parallel Conjunctival Folds and Other Signs and Symptoms of Dry NCT01268735 | University of Zagreb | Phase 4 |
| Completed | Treatment of Meibomian Gland Dysfunction and Evaporative Dry Eye NCT00832130 | TearScience, Inc. | N/A |
| Completed | Long Term Administration Study of OPC-12759 Ophthalmic Suspension NCT00818324 | Otsuka Pharmaceutical Co., Ltd. | Phase 3 |
| Completed | A Prospective, Randomized, Placebo and Active Comparator Controlled Study of CP-690,550 in Subjects With Dry E NCT00784719 | Pfizer | Phase 1 / Phase 2 |
| Completed | Efficacy and Safety Study of ATs in Patients With Dry Eye Syndrome NCT00788229 | Dhp Korea Co., Ltd. | Phase 2 |
| Completed | Comparison of Evaporimetry With the Established Methods of Tear Film Measurement NCT01496482 | University of Zagreb | — |
| Completed | Effects of Sea Buckthorn Oil on Dry Eye NCT00739713 | University of Turku | N/A |
| Completed | Efficacy and Acceptability of Two Lubricant Eye Drops NCT00756678 | Allergan | Phase 4 |
| Completed | Validation of TearLab Osmometer - Human Factor Usability Report NCT00731484 | TearLab Corporation | — |
| Completed | Diagnostic Evaluation of the Tear Film NCT00761917 | TearScience, Inc. | — |
| Completed | Bilateral, Masked Comparison of PEG-400 Based Artificial Tear vs. Systane for Dry Eye Signs, Symptoms & Refrac NCT00620893 | Bp Consulting, Inc | Phase 4 |
| Completed | Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Patients NCT00611403 | Allergan | Phase 2 |
| Terminated | Pilot Study of a Homeopathic Therapy in Combination With Cyclosporin (Restasis) in the Treatment of Dry Eye Di NCT01072526 | University of Missouri-Columbia | Phase 2 |
| Completed | Performance and Acceptance of Optive Versus Hylocomod Eyedrops in Patients With Dry Eye Symptoms NCT00761202 | Allergan | Phase 4 |
| Completed | Refractive Surgery and Optive Compatibility Study NCT00469157 | Innovative Medical | Phase 4 |
| Completed | Late Phase 2 Study of OPC-12759 Ophthalmic Suspension NCT00475319 | Otsuka Pharmaceutical Co., Ltd. | Phase 2 |
| Recruiting | Clinical Applications of Advanced Ophthalmic Imaging NCT03135327 | University of Miami | N/A |
| Unknown | Topical Cyclosporine for the Treatment of Dry Eye in Patients Infected With the Human Immunodeficiency Virus NCT00797030 | Universidade Federal do Rio de Janeiro | Phase 4 |
| Completed | Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome NCT00370747 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | Efficacy of Cyclosporine for the Prevention and Treatment of Dry Eye Symptoms Following LASIK or Photorefracti NCT00349440 | Innovative Medical | Phase 4 |
| Completed | The Effect of Punctal Plugs on Tear Volume and Osmolality NCT00372034 | The University of New South Wales | N/A |
| Completed | Efficacy and Safety Study for Ecabet Ophthalmic Solution for Treating Dry Eye Syndrome NCT00198536 | Bausch & Lomb Incorporated | Phase 2 / Phase 3 |
| Completed | Dose-response Study of OPC-12759 Ophthalmic Suspension NCT00234078 | Otsuka Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Efficacy of T1675 Versus Placebo in Patients With Bilateral Treated Moderate Dry Eye Syndrome NCT00357201 | Laboratoires Thea | Phase 2 |
| Completed | Comparative Study of 0.5% Carboxymethylcellulose With 0.005% Stabilized Oxychlorocomplex (PURITE™) Versus 0.5% NCT00386646 | Chulalongkorn University | Phase 4 |
| Completed | A Parallel Group Phase II Study of KCT-0809 in Patients With Dry Eye Syndromes NCT01692145 | Kissei Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Soothe Versus Refresh NCT00284999 | Pharmaceutical Research Network | Phase 4 |
| Completed | Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-007) NCT00548301 | Sirion Therapeutics, Inc. | Phase 3 |
| Completed | A Study of KCT-0809 in Patients With Dry Eye Syndromes NCT01211951 | Kissei Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | A Late Phase II Study of KCT-0809 in Patients With Dry Eye Syndromes NCT01890941 | Kissei Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Phase 2 Study of KLS-0611 in Patients With Dry Eye Syndromes NCT00721656 | Kissei Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-005) NCT00502073 | Sirion Therapeutics, Inc. | Phase 3 |
| Completed | A Phase II Study of KCT-0809 in Patients With Dry Eye Syndrome NCT01427816 | Kissei Pharmaceutical Co., Ltd. | Phase 2 |
| Completed | Study of Cyclosporine in the Treatment of Dry Eye Syndrome (ST-603-006) NCT00549289 | Sirion Therapeutics, Inc. | Phase 3 |