| Recruiting | An Evaluation of the Safety and Tolerability of Ocular Lubricants NCT07238699 | Alcon Research | N/A |
| Recruiting | Efficacy and Safety of BUFY01 Versus SVS20 in the Treatment of Dry Eye Disease NCT05865379 | TRB Chemedica International SA | N/A |
| Not Yet Recruiting | A Study to Evaluate the Safety and Effectiveness of Perfluorohexyloctane Eye Drops on Treatment of Dry Eye Dis NCT07457021 | Xiamen Ophthalmology Center Affiliated to Xiamen University | — |
| Recruiting | A Study on the Correlation Between Tear Iron Levels and the Severity of Dry Eye Disease. NCT07363824 | Shanghai Changzheng Hospital | — |
| Not Yet Recruiting | Study to Evaluating PRO-240 Ophthalmic Solution Compared to Optive® NCT06375343 | Laboratorios Sophia S.A de C.V. | Phase 1 |
| Recruiting | Vit-A-Vision® Clinical Investigation NCT06596733 | OmniVision GmbH | N/A |
| Recruiting | A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tear Formulation (ABBV-444) Compar NCT07284381 | AbbVie | Phase 3 |
| Withdrawn | A Study to Assess the Long-Term Safety of Lifitegrast/Perfluorohexyloctane Fixed-Dose Combination in Subjects NCT07111013 | Bausch & Lomb Incorporated | Phase 3 |
| Recruiting | Evaluating the Safety, Tolerability, and Efficacy of GRF312 5% in Participants With Dry Eye Disease (DED). NCT07264517 | Instituto Grifols, S.A. | Phase 2 |
| Recruiting | A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease NCT07128628 | Bausch & Lomb Incorporated | Phase 2 |
| 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 | Efficacy and Safety of BUFY02 Versus TRB02 in the Treatment of Dry Eye Disease NCT05865457 | TRB Chemedica International SA | N/A |
| Completed | Phase 2b Controlled Study NCT07140380 | IVIEW Therapeutics Inc. | Phase 2 |
| Recruiting | A Study to Explore Signs, Symptoms, and Biomarkers in Dry Eye Disease Participants Following Anti-inflammatory NCT07025811 | Hoffmann-La Roche | Phase 4 |
| Not Yet Recruiting | A Study to Evaluate the Efficacy and Safety of Treatment With CsA-PG Ophthalmic Gel in Dry Eye Patients NCT06942793 | Zhaoke (Guangzhou) Ophthalmology Pharmaceutical Ltd. | Phase 3 |
| Not Yet Recruiting | Efficacy of Lipid-containing Artificial Tears in the Treatment of Dry Eye NCT06955585 | University Hospital Sestre Milosrdnice | N/A |
| Terminated | Evaluation of the Safety and Tolerability of Ocular Lubricants NCT06571656 | Alcon Research | N/A |
| Not Yet Recruiting | Characterization of Subjective Discomfort in Patients With Tear Dysfunction NCT06819631 | IRCCS Azienda Ospedaliero-Universitaria di Bologna | — |
| Completed | A Study to Evaluate 0.003% AR-15512 Safety and Drop Attributes NCT06660290 | Alcon Research | Phase 3 |
| Not Yet Recruiting | Effect of Artificial Tears on Ocular Biometry Parameters NCT06656403 | He Eye Hospital | N/A |
| Terminated | Evaluation of Reflex Tear Production NCT06565624 | Alcon Research | N/A |
| Completed | A Study Designed to Evaluate Tear Production NCT06544707 | Alcon Research | Phase 3 |
| Completed | A Study to Investigate the Effect of 0.003% AR-15512 on Subjects With Dry Eye Disease NCT06544694 | Alcon Research | Phase 3 |
| Completed | Effectiveness of Dry Eye Treatment With Diquafosol Sodium 3% After Phaco Surgery NCT07122635 | Le Xuan Cung | — |
| Completed | Study of Safety and Performance of a Novel Ocular Lubricant in Subjects With Dry Eye Disease NCT06444516 | Alcon Research | N/A |
| Not Yet Recruiting | iTear Single-center, Open-label, Single-arm Study NCT06525961 | The University of Hong Kong | Phase 4 |
| Completed | Efficacy of Twinkle Eyez Supplementation in Improving Ocular Health and Immunity NCT06574685 | Ecolite Group | N/A |
| Completed | IVW-1001 Phase 1/2 in Subjects With Dry Eye Disease NCT06400459 | IVIEW Therapeutics Inc. | Phase 1 / Phase 2 |
| Completed | A Trial to Assess the Safety and Efficacy of Subjects With Dry Eye Disease NCT06493604 | Aldeyra Therapeutics, Inc. | Phase 3 |
| Completed | Preoperative iLux on Cataract Surgery Derived Dry Eye Disease Due to Meibomian Gland Dysfunction NCT06483750 | George Washington University | N/A |
| Active Not Recruiting | A Phase 3 Study to Evaluate AZR-MD-001 in Patients with Abnormal Meibomian Gland Function and Dry Eye Disease NCT06329791 | Azura Ophthalmics | Phase 3 |
| Completed | Clinical Study to Evaluate the Safety and Tolerability of PRO-229 Ophthalmic Solution Compared to Lagricel® Of NCT06370585 | Laboratorios Sophia S.A de C.V. | Phase 1 |
| Completed | A Clinical Trial to Assess the Safety and Efficacy of Subjects With Dry Eye Disease NCT06424444 | Aldeyra Therapeutics, Inc. | Phase 3 |
| Completed | A Clinical Trial to Evaluate the Corneal Endothelial Health of DED Subjects Treated With Cyclosporine NCT06329661 | Novaliq GmbH | Phase 4 |
| Completed | A Clinical Trial to Assess the Efficacy and Safety of Subjects With Dry Eye Disease NCT06389214 | Aldeyra Therapeutics, Inc. | Phase 3 |
| Unknown | Neurological Dry Eye Study Stimulating Both Lacrimal and Vagus Nerves NCT06271005 | Genetic Disease Investigators | N/A |
| Completed | Study of INV-102 Ophthalmic Solution in Adults With Moderate to Severe Dry Eye Disease NCT06370039 | Invirsa, Inc. | Phase 2 |
| Enrolling By Invitation | Efficacy of 0.05% Cyclosporine A Eye Drops Combined With Absorbable Tear Duct Plugs in the Treatment of Dry Ey NCT07171710 | Tianjin Eye Hospital | N/A |
| Recruiting | The Pattern of Dry Eye Disease After Cataract Surgery NCT06298890 | Lithuanian University of Health Sciences | — |
| Active Not Recruiting | A Study of TL-925 Ophthalmic Emulsion as a Treatment for Dry Eye Disease NCT06225973 | Telios Pharma, Inc. | Phase 2 |
| Recruiting | Evaluation of the Effectiveness of a Community Health Management Program for Dry Eye Disease in Middle-Aged an NCT06443554 | Fujian University of Traditional Chinese Medicine | N/A |
| Completed | A Safety and Efficacy Study of 2 Dosing Regimens of Recombinant Human Nerve Growth Factor (rhNGF) Eye Drop Sol NCT06244316 | Dompé Farmaceutici S.p.A | Phase 2 |
| Unknown | Topical Statin Eye Drop in the Management of the Dry Eye NCT06208384 | Shahid Beheshti University of Medical Sciences | Phase 1 / Phase 2 |
| Unknown | Efficacy and Safety of USL for Dry Eye Disease NCT06016010 | Chan-Sik Kim | Phase 2 |
| Unknown | Corneal and Tear Film Changes in Chinese Patients With Type 2 Diabetes NCT06218992 | He Eye Hospital | — |
| Unknown | Safety and Efficacy of ST-100 (Vezocolmitide) Ophthalmic Solution 60 μg/ml Ophthalmic Solution in Subjects Dia NCT06178679 | ORA, Inc. | Phase 3 |
| Completed | Safety and Efficacy of Licaminlimab Ophthalmic Solution for the Treatment of Dry Eye Disease NCT05896670 | Oculis | Phase 2 |
| Unknown | Assess the Effects of Spectacles or Orthokeratology on Dry Eye Parameters in Children and Adolescents. NCT06023108 | He Eye Hospital | N/A |
| Unknown | Eye Mask on Sleep Quality and Tear Layer Function in Patients With Dry Eye Disease NCT06016166 | Hamideh Sabbaghi | N/A |
| Completed | Evaluation of Miebo (Perfluorohexyloctane) Eyedrops in Habitual Contact Lens Wearers NCT06176651 | Gordon Schanzlin New Vision | Phase 4 |
| Active Not Recruiting | Clinical Study Evaluating Nordlys™ SWT IPL for Dry Eye Disease (DED) Due to MGD NCT06064071 | Candela Corporation | N/A |
| Unknown | Study of Application of Pulse Electrical Stimulation Around Eye in Dry Eye Disease Patients Who Are Scheduled NCT06120348 | Nu Eyne Co., Ltd. | N/A |
| Unknown | The Effects and Safety of Topical Spironolactone Ophthalmic Solution, 0.005 mg/cc in Subjects With Dry Eye Dis NCT05995392 | Richard W Yee, MD | EARLY_Phase 1 |
| Withdrawn | Examining the Clinical Characteristics, Treatment Patterns, Real-world Effectiveness, and Healthcare Resource NCT05857748 | Novartis Pharmaceuticals | — |
| Completed | Evaluation of Safety and Tolerability of Investigational Ocular Lubricants NCT05888519 | Alcon Research | N/A |
| Completed | Efficacy and Safety Evaluation of Tavilermide Ophthalmic Solution for the Treatment of Dry Eye NCT05848128 | Mimetogen Pharmaceuticals USA, Inc. | Phase 3 |
| Completed | Effect of Sunflower Lecithin Supplementation on Meibomian Gland Function in Adults With Dry Eye Disease NCT06058559 | George Washington University | N/A |
| Completed | Improving Drop Instillation Comfort of a Cyclosporine A Solution NCT05957211 | University of Waterloo | N/A |
| Suspended | QST for Corneal Nerve Function NCT05758753 | Tufts Medical Center | N/A |
| Completed | Dry Eye Disease and Retinal Nerve Fiber Layer Thickness in Chronic Smokers NCT07028736 | Cairo University | — |
| Completed | The Study Evaluating the Efficacy and Safety of OK-101 in Subjects With Dry Eye Disease NCT05759208 | Okyo Pharma Ltd | Phase 2 |
| Completed | Prospective Evaluation of Efficacy and Safety of an Intense Pulsed Light Device to Treat Dry Eye Disease" NCT06349356 | Quantel Medical | N/A |
| Completed | HU007 in Patients with Dry Eye Syndrome NCT05743764 | Huons Co., Ltd. | Phase 3 |
| Terminated | A Multi-Centre, Randomised, Controlled, Masked Phase 2 Study of the Safety and Efficacy of KIO-101 Ophthalmic NCT05629364 | Kiora Pharmaceuticals, Inc. | Phase 2 |
| Unknown | Management of the Ocular Surface With Preservative-Free Lubricants in Patients With Dry Eye NCT06162442 | Tecnoquimicas | — |
| Unknown | Idroflog® for Treatment of Dry Eye Disease (IDROFLOG) NCT05724056 | Alfa Intes Industria Terapeutica Splendore s.r.l. | N/A |
| Unknown | Safety and Efficacy of Pluripotent Stem Cell-derived Mesenchymal Stem Cell Exosome (PSC-MSC-Exo) Eye Drops Tre NCT05738629 | Second Affiliated Hospital, School of Medicine, Zhejiang University | Phase 1 / Phase 2 |
| Completed | Assessment of the Safety and Efficacy of BRM421 Ophthalmic Solutions in Dry Eye Subjects. NCT05695781 | BRIM Biotechnology Inc. | Phase 3 |
| Completed | A Study of TL-925 as a Treatment for Dry Eye Disease NCT05745064 | Telios Pharma, Inc. | Phase 2 |
| Completed | Phase II Study of SHJ002 Sterile Ophthalmic Solution Compared With Vehicle in Participants With Dry Eye Diseas NCT05486728 | Dreamhawk Vision Biotech, Inc. | Phase 2 |
| Unknown | Intense Regulated Pulse Light Therapy in Dry Eye Disease NCT05553561 | Menoufia University | N/A |
| Completed | Evaluation of the Tolerability and Efficacy of CWT-f-002 Lubricant Eye Drops NCT05660681 | Calm Water Therapeutics LLC | N/A |
| Completed | Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of OC-01 in Adult Chinese With Dry Eye Disease NCT05576415 | Corxel Pharmaceuticals | Phase 1 |
| Completed | PMCF Study to Evaluate Performance and Safety of "Xanoftal Next" NCT05829499 | C.O.C. Farmaceutici S.r.l. | N/A |
| Unknown | Assessment of Efficacy and Safety of the Use of Two Eye Gel Products Containing 5% Dexpanthenol in Patients Wi NCT06210373 | Fidia Farmaceutici s.p.a. | N/A |
| Completed | A Long-Term Safety Study Evaluating the Safety and Systemic Exposure of AR-15512 NCT05493111 | Aerie Pharmaceuticals | Phase 3 |
| Unknown | Effectiveness of Diquafosol Prophylactic Therapy to Prevent Dry Eye Disease for Cataract Surgery Patients in I NCT06146881 | Indonesia University | Phase 2 |
| Completed | PMCF Study to Evaluate Performance and Safety of "HPMC-based Eyedrops" Used to Relieve Dry Eye Symptoms NCT05825599 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | Study of INV-102 Ophthalmic Solution in Adults With Moderate Symptomatic Dry Eye Disease NCT05586152 | Invirsa, Inc. | Phase 1 / Phase 2 |
| Unknown | A Randomized, Controlled, Double-masked, Investigator-initiated Trial to Evaluate Tear Film Quality and Stabil NCT05514041 | Stephenson Eye Associates | Phase 4 |
| Completed | PMCF Study to Evaluate Performance and Safety of "Distilled Waters-based Eyedrops" Used to Relieve Dry Eye Sym NCT05825586 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | A Study for Evaluation of the Efficacy and Safety of SI-614 Ophthalmic Solution in Patient With Dry Eye NCT05411367 | Seikagaku Corporation | Phase 3 |
| Completed | Study of SY-201 Ophthalmic Solution in Subjects With Dry Eye Disease NCT05370495 | Seinda Pharmaceutical Guangzhou Corporation | Phase 1 / Phase 2 |
| Completed | Clinical Trial to Evaluate the Efficacy and Safety of OC-01 (Varenicline) Nasal Spray on Signs and Symptoms of NCT05378945 | Corxel Pharmaceuticals | Phase 3 |
| Completed | Feasibility of IPL Combined With RF for Treatment of DED Due to MGD NCT05487547 | Lumenis Be Ltd. | N/A |
| Completed | Study Evaluating the Safety and Efficacy of AR-15512 (COMET-3) NCT05360966 | Aerie Pharmaceuticals | Phase 3 |
| Completed | A Study to Confirm the Efficacy and Safety of K-161 Ophthalmic Solution for Treatment of Moderate to Severe Dr NCT05403827 | Kowa Research Institute, Inc. | Phase 3 |
| Completed | PMCF Study to Evaluate Performance and Safety of "Hyaluronic Acid (HA)-Based Eyedrops" Used to Relieve Dry Eye NCT05807360 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | A Study of AG-80308 in Dry Eye Patients NCT05372107 | Allgenesis Biotherapeutics Inc. | Phase 1 |
| Completed | PMCF Study to Evaluate Performance and Safety of "CLHA-based Eyedrops" Used to Improve Lacrimal Abnormalities NCT05823961 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | PMCF Study to Evaluate Performance and Safety of "Optrex Double Action Soothing and Lubricating Drops" NCT05824000 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | Burden of Illness and Treatment Assessment of Patients With Dry Eye Disease: A Cross-Sectional Survey of Real- NCT06018571 | Novartis Pharmaceuticals | — |
| Completed | Vizol S Lipid Balance Efficacy and Safety Study in Patients With Dry Eye NCT06323395 | Jadran Galenski laboratorij d.d. | Phase 3 |
| Completed | Study Evaluating the Safety and Efficacy of AR-15512 NCT05285644 | Aerie Pharmaceuticals | Phase 3 |
| Recruiting | 2177GCCC:ID'Ing tx Targets and Biomarkers for Ocular Surface Disease in Pt w/ oGVHD NCT04946721 | University of Maryland, Baltimore | — |
| Completed | Diamond Bur Microblepharoexfoliation, Intense Pulse Light and Meibomian Gland Expression for Evaporative Dry E NCT05857579 | University of Seville | N/A |
| Completed | PMCF Study to Evaluate Performance and Safety of "Ocular Drops Based Upon Carmellose" Used to Relieve Dry Eye NCT05825352 | C.O.C. Farmaceutici S.r.l. | N/A |
| Completed | Safety Study of Tivanisiran to Treat Dry Eye NCT05310422 | Sylentis, S.A. | Phase 3 |
| Unknown | Comparison of Two Types of Artificial Tears NCT05356728 | The Norwegian Dry Eye Clinic | N/A |
| Completed | Efficacy of Riboflavin-Enhanced Hyaluronic Acid Eye Drops in Treating Dry Eye Disease NCT06122428 | University of Naples | — |
| Completed | Study to Evaluate Safety and Efficacy of Cenegermin (Oxervate®) vs Vehicle in Severe Sjogren's Dry Eye Disease NCT05136170 | Dompé Farmaceutici S.p.A | Phase 3 |
| Completed | A Study to Evaluate the Safety, Tolerability, and Efficacy of A197 in Subjects With Dry Eye Disease NCT05238597 | Aramis Biosciences, Inc. | Phase 2 |
| Completed | Systane Hydration in Subjects Undergoing Cataract Surgery NCT05056233 | Alcon Research | N/A |
| Completed | Sphenopalatine Ganglion Stimulation for Ocular and Oral Dryness NCT05187533 | Instituto Universitario de Oftalmobiología Aplicada (Institute of Applied Ophthalmobiology) - IOBA | N/A |
| Completed | Safety and Efficacy of Pilocarpine Ophthalmic Topical Cream for the Treatment of Dry Eye Disease NCT05119920 | Glaukos Corporation | Phase 2 |
| Completed | Safety of Tinted Soft Scleral Eye Shields When IPL is Applied on Eyelids NCT05168670 | Lumenis Be Ltd. | N/A |
| Completed | Study Evaluating Techniques for Measuring Tear Production NCT05497479 | Aerie Pharmaceuticals | Phase 1 |
| Completed | Hyaluronic Acid-containing Artificial Tears in Post-cataract Surgery Dry Eye Disease NCT06221345 | Chang Gung Memorial Hospital | Phase 4 |
| Unknown | IIT Assessing OC-01Nasal Spray on Symptoms of DED Following CXL NCT05136924 | Vance Thompson Vision - MT | Phase 2 |
| Completed | Efficacy and Safety of 20% and 100% Autologous Serum Eye Drops in Patients With Severe Dry Eye Disease (AST) NCT07469865 | University Hospital, Ghent | N/A |
| Completed | Ditefossol Sodium 3% Eye Drops in Patients With Dry Eye NCT06560580 | Tianjin Eye Hospital | N/A |
| Completed | Systane Complete Multi-symptom Relief NCT05056155 | Alcon Research | N/A |
| Completed | Strip Meniscometry in Dry Eye Evaluation NCT06120894 | University Hospital Olomouc | — |
| Completed | Investigator Initiated Study to Assess the Efficacy of OC-01 (Varenicline) Nasal Spray on Signs and Symptoms o NCT05082974 | Vance Thompson Vision ND | Phase 3 |
| Completed | Evaluation of the Safety, Tolerability and Efficacy of iNexin™ for the Treatment of the Signs and Symptoms Ass NCT05031806 | Xequel Bio, Inc. | Phase 1 |
| Completed | The Evaluation of the Transcutaneous Electrical Stimulation Medical Device's Safety and Effectiveness in Treat NCT05203796 | Nu Eyne Co., Ltd. | N/A |
| Recruiting | Transcutaneous Auricular Vagus Nerve Stimulation in Dry Eye NCT06696625 | Beijing Tongren Hospital | N/A |
| Unknown | Corneal Thickness Changes in Patient Undergoing Dry Eye Managment NCT04970329 | University of Faisalabad | N/A |
| Unknown | Efficacy of Blue Wavelength in Managing Dry Eye NCT04965974 | University of Faisalabad | N/A |
| Recruiting | Transcutaneous Auricular Vagus Nerve Stimulation in Dry Eye Disease NCT04673643 | Beijing Tongren Hospital | Phase 2 |
| Completed | Tivanisiran for Dry Eye in Subjects With Sjögren's Syndrome NCT04819269 | Sylentis, S.A. | Phase 3 |
| Completed | Study of ST-100 as Treatment for Dry Eye Disease NCT05241470 | Stuart Therapeutics, Inc. | 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 | Efficacy and Safety of SHR8028 Eye Drops for the Treatment of Dry Eye Disease NCT05841043 | Jiangsu HengRui Medicine Co., Ltd. | Phase 3 |
| Completed | Comparison of Mucin Levels at the Ocular Surface of Visual Display Users With and Without Dry Eye Disease NCT05604651 | Peking University Third Hospital | — |
| Completed | Safety and Efficacy of Two Different Concentrations (0.5% and 1%) of Progesterone Topical Gel Compared to Plac NCT04645446 | SIFI SpA | Phase 2 |
| Completed | Comparison of Efficacy Between 100% Platelet-rich Plasma and 100% Serum Eye Drops in Dry Eye Disease NCT04683796 | Mahidol University | Phase 3 |
| Unknown | Multimodal Screening of Dry Eye Disease NCT04235400 | Assistance Publique - Hôpitaux de Paris | — |
| Completed | A Multi-Center, Double-Masked, Randomized, Vehicle-Controlled, Parallel-Group Clinical Trial Evaluating the Sa NCT04735393 | Aldeyra Therapeutics, Inc. | Phase 3 |
| Unknown | Comprehensive Study on Dry Eye and Ocular Surface Disease Prior and After Cataract Surgery NCT04711642 | Fundación Oftalmológica Los Andes | Phase 3 |
| Completed | A Research Study To See How Well an Eye Drop, SURF-100 (A Mycophenolic Acid/Betamethasone Sodium Phosphate Com NCT04734197 | Surface Ophthalmics, Inc. | Phase 2 |
| Completed | Research Study To See How Well An Eye Drop (SURF-200) Works, What Side Effects There Are, And To Compare It Wi NCT04734210 | Surface Ophthalmics, Inc. | Phase 2 |
| Unknown | Pre-Surgical Ocular Surface Treatment With Intracanalicular Dexamethasone Insert And Effect On Intraocular Len NCT04530864 | Prism Vision Group | Phase 4 |
| Completed | ESSENCE 2: CyclASol for the Treatment of Signs and Symptoms of Dry Eye Disease (DED) NCT04523129 | Novaliq GmbH | Phase 3 |
| Completed | Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave S NCT04567329 | Bausch & Lomb Incorporated | Phase 3 |
| Completed | A Phase 2b Study Evaluating the Safety and Efficacy of AR-15512 Ophthalmic Solution for the Treatment of Dry E NCT04498182 | Aerie Pharmaceuticals | Phase 2 |
| Completed | Study on Safety and Performance of an Artificial Tear in Dry Eye Treatment in Subjects With Ocular Surface Inf NCT04633863 | MD Italy | N/A |
| Recruiting | Ocular Microbiome and Immune System in Dry Eyes NCT04658238 | Insel Gruppe AG, University Hospital Bern | — |
| Completed | Study to Evaluate the Efficacy and Safety of CKD-352 NCT04548427 | Chong Kun Dang Pharmaceutical | Phase 3 |
| Completed | Changes in Tear Lipid Layer Thickness After Short Exposure to Light Emitting Diode Displays NCT05003128 | National Cheng-Kung University Hospital | N/A |
| Completed | Effect of Cequa™ in Subjects With Dry Eye Disease NCT04357795 | Sun Pharmaceutical Industries Limited | Phase 4 |
| Completed | Study to Evaluate the Safety, Tolerability, and Efficacy of OTX-CSI in Subjects With Dry Eye Disease. NCT04362670 | Ocular Therapeutix, Inc. | Phase 1 / Phase 2 |
| Completed | Evaluating the Efficacy of Dry Eye (DE) Disease Treatment Using Novel Tear Film Imager (TFI) NCT04670263 | Adom Advanced Optical Technologies Ltd. | Phase 2 / Phase 3 |
| Completed | A Study of the Drugs AGN-242428 and AGN-231868 in Participants With Dry Eye Disease NCT04030962 | AbbVie | Phase 1 / Phase 2 |
| Completed | Application of Pulse Electrical Stimulation Around Eye in Dry Eye Disease Patients Scheduled for LASEK Surgery NCT05271422 | Nu Eyne Co., Ltd. | N/A |
| Completed | Efficacy and Safety of PL9643 Ophthalmic Solution in Subjects With Dry Eye NCT04268069 | ORA, Inc. | Phase 2 |
| Completed | Phase 1/2a Safety and Efficacy of ALY688 Ophthalmic Solution in Subjects With Dry Eye Disease NCT04201574 | Allysta Pharmaceutical | Phase 1 / Phase 2 |
| Unknown | Refractory Meibomian Gland Dysfunction and Plasma Jet NCT04608942 | Federal University of São Paulo | N/A |
| Completed | Safety, PK and Efficacy Study of SJP-0132 in Subjects With Dry Eye Disease NCT04139122 | Senju Pharmaceutical Co., Ltd. | Phase 1 / Phase 2 |
| Completed | The Ocular Microbiome in Patients With Dry Eye Disease NCT04656197 | Insel Gruppe AG, University Hospital Bern | — |
| Completed | Concentration of Ofloxacin Into the Aqueous Humour of Patients With Dry Eye Disease NCT05213156 | University Hospital of Patras | Phase 4 |
| Completed | A Study Assessing the Safety, Efficacy, and Optimum Dosage of K-161 in Subjects With Moderate to Severe Dry Ey NCT04084483 | Kowa Research Institute, Inc. | Phase 2 |
| Completed | Clinical Trial to Evaluate the Chronic Efficacy of OC-01 Nasal Spray on Signs of Dry Eye Disease (The MYSTIC S NCT03873246 | Oyster Point Pharma, Inc. | Phase 2 |
| Unknown | Self-care Management Program for Dry Eye Disease Patients Using the heiQ NCT03467490 | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's | N/A |
| Completed | Efficacy of OC-01 Nasal Spray on Goblet Cell and Meibomian Gland Stimulation NCT03688802 | Oyster Point Pharma, Inc. | Phase 2 |
| Completed | Study to Assess Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of Palovarot NCT04762355 | Clementia Pharmaceuticals Inc. | Phase 1 |
| Completed | Evaluation of the Efficacy of OC-01 Nasal Spray on Signs and Symptoms of Dry Eye Disease NCT03636061 | Oyster Point Pharma, Inc. | Phase 2 |
| Completed | Evaluation of the Efficacy of OC-02 Nasal Spray on Signs and Symptoms of Dry Eye Disease (the RAINIER Study) NCT03633461 | Oyster Point Pharma, Inc. | Phase 2 |
| Completed | Effect of Topical Naltrexone Ophthalmic Solution on the Signs and Symptoms of Dry Eye in Diabetic Subjects NCT03660475 | Sassani, Joseph S., MD, MHA | Phase 2 |
| Completed | Study of Efficacy and Tolerability of SYSTANE Complete in Patients With Dry Eye Disease NCT03492541 | Alcon Research | N/A |
| Completed | Clinical Efficacy of H.P. Acthar Gel 80 U/ml to Improve the Signs and Symptoms in Subjects With Dry Eye Diseas NCT03287635 | Toyos Clinic | Phase 4 |
| Unknown | Investigating the Effect of At Home Thermal Therapy on Dry Eye Patients With Meibomian Gland Dysfunction NCT03291704 | UMay Care Inc. | N/A |
| Completed | Clinical Trial to Evaluate the Efficacy of OC-02 Nasal Spray on Signs and Symptoms of Dry Eye Disease (The PEA NCT03452397 | Oyster Point Pharma, Inc. | Phase 2 |
| Withdrawn | A Dose-Finding Study Comparing InSite Vision, Inc. 101 to Vehicle and DuraSite Alone for Dry Eye Disease NCT01478555 | Sun Pharmaceutical Industries Limited | Phase 2 |
| Completed | CyclASol for the Treatment of Signs and Symptoms of Dry Eye Disease (DED) NCT03292809 | Novaliq GmbH | Phase 2 / Phase 3 |
| Completed | Assessing Safety and Efficacy of DE-089 Ophthalmic Solution in Patients With Dry Eye Disease NCT03216096 | Santen Pharmaceutical Co., Ltd. | Phase 1 |
| Completed | HELIX, a Double-masked Study of SYL1001 in Patients With Moderate to Severe Dry Eye Disease (DED) NCT03108664 | Sylentis, S.A. | Phase 3 |
| Completed | Femtosecond Small Incision Lenticular Extraction in Comparison to Femtosecond Laser Insitu Keratomileusis Rega NCT04477421 | Al-Rasheed University College | N/A |
| Completed | Influence of Perfluorohexyloctane (NovaTears) on Tear Film Thickness in Patients With Mild to Moderate Dry Eye NCT03048526 | Novaliq GmbH | N/A |
| Unknown | Fingerprick Autologous Blood (FAB) in Mebomian Gland Dysfunction (MGD) NCT02943382 | Bedford Hospital NHS Trust | N/A |
| Completed | Pilot Study for Investigating the Effect of the Bruder Eye Hydrating Compress on Contact Lens Discomfort in Co NCT02848222 | University of Alabama at Birmingham | N/A |
| Terminated | Study of the Pharmacodynamic Activity of P-321 Ophthalmic Solution Compared to Placebo in Subjects With Dry Ey NCT02824913 | Parion Sciences | Phase 2 |
| Terminated | Evaluation of P-321 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye Disease NCT02831387 | Parion Sciences | Phase 2 |
| Completed | In Vivo Confocal Microscopic Analysis of Corneal Nerve Changes After ProKera Slim® for Dry Eye NCT02764814 | BioTissue Holdings, Inc | N/A |
| Completed | A Study to Evaluate Efficacy and Safety of Lifitegrast in Subjects With Dry Eye (OPUS-3) NCT02284516 | Shire | Phase 3 |
| Completed | Optical Coherence Tomography of Tear Film Dynamics In-Vivo NCT02554084 | University of Rochester | N/A |
| Completed | Phase 2/3 Dose-Ranging Study of the Safety and Efficacy of OTX-101 in the Treatment of Keratoconjunctivitis Si NCT02254265 | Sun Pharmaceutical Industries Limited | Phase 2 / Phase 3 |
| Completed | Study of the Safety and Tolerability of P 321 Ophthalmic Solution in Subjects With Dry Eye Disease NCT02242032 | Parion Sciences | Phase 1 |
| Completed | The Influence of PRN Dry Eye Omega-3 Nutritional Regimen on Tear Osmolarity In Cases Of Dry Eye Disease NCT02260960 | Physician Recommended Nutriceuticals | Phase 2 / Phase 3 |
| Completed | The Utility of IVCM to Assess Cellular Response and Efficacy of Long-term Topical Steroid Treatment in Patient NCT02120079 | Tufts Medical Center | Phase 4 |
| Completed | Ocular Surface Immune Response in Dry Eye Disease NCT02042820 | Tufts Medical Center | — |
| Withdrawn | A Phase IV, Randomized, Parallel Group, Investigator-Masked Evaluation of the Effect of Loteprednol Etabonate NCT02028312 | Edward Holland, MD | Phase 4 |
| Completed | NovaTears® Eye Drops Observational Study NCT02111928 | Novaliq GmbH | — |
| Completed | A Study to Compare the Safety and Efficacy of A New Eye Drop Formulation With OPTIVE™ in Subjects With Dry Eye NCT01664949 | Allergan | Phase 3 |
| Completed | A Phase 3 Study to Evaluate the Efficacy of Lifitegrast in Subjects With Dry Eye NCT01743729 | Shire | Phase 3 |
| Completed | Safety Study of Lifitegrast to Treat Dry Eye NCT01636206 | Shire | Phase 3 |
| Completed | Evaluation of Ocular Comfort With ISTA Tears vs Systane NCT01650584 | Bausch & Lomb Incorporated | N/A |
| Completed | Systane Ultra Versus Maxidex Versus Saline NCT01775540 | Icahn School of Medicine at Mount Sinai | N/A |
| Completed | A Study Assessing the Safety and Efficacy of DE-101 Ophthalmic Suspension in Dry Eye Patients NCT01468168 | Santen Inc. | Phase 2 |
| Completed | Safety and Efficacy Study of SAR 1118 to Treat Dry Eye Conducted in a Controlled Adverse Environment (CAE) (OP NCT01421498 | Shire | Phase 3 |
| Completed | Diurnal Variation in Tear Osmolarity NCT01321424 | Ophthalmic Consultants of Long Island | — |
| Completed | Evaluation of Anti-Inflammatory Treatment in Dry Eye Patients NCT01276223 | Alcon Research | Phase 2 |
| Unknown | Dry Eye Disease in the Vitamin D and Omega-3 Trial (VITAL) NCT01880463 | Brigham and Women's Hospital | N/A |
| Completed | A Four Week Study of Azithromycin Ophthalmic Solution, 1% Versus Placebo in Subjects With Dry Eye Disease NCT01014078 | Merck Sharp & Dohme LLC | Phase 4 |
| Completed | Physician's Evaluation of Cyclosporine Ophthalmic Emulsion 0.05% NCT00827255 | Allergan | — |
| Completed | The Effects of Diquafosol Tetrasodium Ophthalmic Solution, 2% in Subjects With Dry Eye Disease (P08637) NCT00831662 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | Exploratory Study Comparing Signs and Symptoms in Patients With Ocular Hypertension or Glaucoma Using Xalatan NCT00799682 | Ophthalmic Consultants of Long Island | Phase 4 |
| Completed | Safety and Efficacy of an Ophthalmic Solution in Dry Eye Disease NCT00758784 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | Clinical Pharmacological Study of AL-43546 Ophthalmic Product in Subjects With Shortened Tear Film Break Up Ti NCT00760045 | Alcon Research | Phase 2 |
| Unknown | The Evaluation of Thiol Redox Status in Conjunctiva of Dry Eye Patients NCT00718926 | Meiji University of Oriental Medicine | — |
| Completed | Efficacy Study of Ecabet Ophthalmic Solution in Dry Eye Disease NCT00667004 | Bausch & Lomb Incorporated | Phase 2 |
| Completed | Study of the Effect of Diquafosol Tetrasodium Ophthalmic Solution, 2% Versus Placebo in Dry Eye Subjects (P086 NCT00600288 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | Tear Film Stability After Instillation of Over-the-Counter (OTC) Artificial Drops NCT00610480 | University of Texas Southwestern Medical Center | N/A |
| Completed | Bromfenac 0.09% vs Ketorolac 0.4% for Cyclosporine Induction Phase NCT00520260 | Florida Eye Microsurgical Institute | Phase 4 |
| Completed | The Relationship of Residence Time and Visual Effect of Optive and Systane in Dry Eye Subjects NCT00553579 | Southern California College of Optometry at Marshall B. Ketchum University | — |
| Completed | Safety and Efficacy Assessment of Vismed® (Sodium Hyaluronate) for the Treatment of Dry Eye Syndrome NCT00599716 | Lantibio | Phase 3 |
| Completed | Multicenter, Randomized, Controlled Study of the Effect of Lotemax on Initiation of Dry Eye Treatment With Res NCT00407043 | Ophthalmic Consultants of Long Island | Phase 4 |
| Completed | The Visual Effect of an Investigational Artificial Tear in the Tear Layer. NCT00395759 | Southern California College of Optometry at Marshall B. Ketchum University | N/A |
| Completed | Study of Diquafosol Tetrasodium Ophthalmic Solution in Subjects With Dry Eye Disease NCT00403975 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | Study of INS365 Ophthalmic Solution in Subjects With Dry Eye Disease NCT00404131 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | Study of INS365 Ophthalmic Solution in Subjects With Dry Eye Disease NCT00403715 | Merck Sharp & Dohme LLC | Phase 3 |
| Completed | A Study of INS365 Ophthalmic Solution in Patients With Moderate to Severe Dry Eye Disease NCT00679718 | Merck Sharp & Dohme LLC | Phase 2 |
| Completed | A Study to Determine the Safety and Tolerability of Escalating Doses of INS365 Ophthalmic Solution NCT00680108 | Merck Sharp & Dohme LLC | Phase 2 |