| Completed | Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens NCT06377514 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Unknown | Aberrometry and Straylight Measurements as an Indication for Cataract Surgery NCT06257914 | Amphia Hospital | — |
| Completed | A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens NCT06250322 | Johnson & Johnson Surgical Vision, Inc. | — |
| Completed | Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL NCT05991960 | Johnson & Johnson Surgical Vision, Inc. | — |
| Completed | User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL NCT06005675 | Johnson & Johnson Surgical Vision, Inc. | — |
| Completed | PROOF-OF-CONCEPT STUDY FOR NEW INTRAOCULAR LENS, MODEL C0002 NCT05531292 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Completed | Clinical Investigation of Healon EndoCoat Ophthalmic Viscosurgical Device (OVD) NCT05575063 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Terminated | Clinical Investigation of the TECNIS® Next-Generation Intraocular Lens, Model DEN00V NCT05574959 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Completed | A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Produ NCT05394324 | Johnson & Johnson Surgical Vision, Inc. | — |
| Completed | A Real-World Study for the TECNIS Synergy™ Intraocular Lens NCT05090826 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Completed | A Real-World Study in China for the TECNIS Eyhance™ Intraocular Lens NCT05090813 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Completed | Evaluation of the TECNIS Symfony® Toric Intraocular Lens NCT05053399 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Completed | Clinical Results of a Monofocal Aspheric Bitoric Intraocular Lens With Plate Haptics in Hyperopic Eyes (HIPER- NCT05058274 | OFTALVIST (Oftalmología Vistahermosa S.L) | — |
| Completed | A Post-Market Evaluation of LipiFlow Treatment in Cataract Surgery Practice NCT03708367 | Johnson & Johnson Surgical Vision, Inc. | N/A |
| Terminated | The Incidence of Glistenings in the 2017 Intraocular Lenses Made by Alcon and Abbott Medical Optics NCT03409185 | University of Toronto | N/A |
| Terminated | Cataract Refractive Suite Study NCT02974140 | Alcon, a Novartis Company | N/A |
| Completed | Clinical Investigation of Corneal Incision Size After Intraocular Lens (IOL) Implantation NCT02826421 | Alcon Research | N/A |
| Completed | Clinical Investigation of Visual Function After Bilateral Implantation of Two Presbyopia-Correcting Trifocal I NCT02691741 | Alcon Research | N/A |
| Withdrawn | Cataract Surgery in Indian Patients With or Without LenSx® Laser NCT02605408 | Alcon Research | — |
| Completed | Clinical Evaluation of the Lenstec SBL-3 Multifocal Intraocular Lens NCT02487160 | Lenstec Incorporated | Phase 3 |
| Completed | Comparison of Centurion® Vision System With Balanced Tip and the Infiniti® Vision System With the Mini Flared NCT02502526 | Alcon Research | N/A |
| Completed | Endothelial Cell Loss After Phacoemulsification Intra and Supracapsular NCT02535819 | Centre Hospitalier Régional Metz-Thionville | N/A |
| Completed | A Real-World Registry to Investigate the Performance of LenSx® Laser in Chinese Patients NCT02396719 | Alcon Research | — |
| Unknown | Manual Small Incision Cataract Surgery Outcomes in an Educational Setting NCT02277314 | University of Arizona | N/A |
| Withdrawn | Study of the Effect of Aspheric Lenses in Patients With Fuch's Dystrophy NCT02109276 | Queen's University | N/A |
| Withdrawn | VIGADEXA Gel Compared to VIGADEXA Solution Following Cataract Surgery NCT01515826 | Alcon Research | Phase 3 |
| Terminated | Imaging Lens Deposits in Exfoliation Syndrome NCT02042703 | Duke University | — |
| Completed | The Efficacy and Safety of IBI-10090 for the Treatment of Inflammation Associated With Cataract Surgery NCT02006888 | ICON Bioscience Inc | Phase 3 |
| Unknown | Eye Drop Application Monitor, Pilot Study NCT02639845 | Alexander Eaton | — |
| Completed | Clinical Research of Femtosecond Laser-Assisted Cataract Surgery NCT02492659 | Wenzhou Medical University | N/A |
| Completed | Comparison of Two Phacoemulsification-methods: Low Fluidic EasyTip 2.2mm vs. High Fluidic EasyTip 2.2mm NCT01936714 | Medical University of Vienna | N/A |
| Completed | Comparison of the Effectiveness of Povidone-iodine in Reducing Conjunctival Bacterial Load Prior to Cataract S NCT01898728 | McMaster University | N/A |
| Completed | A Clinical Outcome Study of Two Multifocal Intraocular Lenses (IOL) in Cataract Patients NCT01684007 | Alcon Research | N/A |
| Completed | Comparison of Two Phacoemulsification-methods: HF EasyTip 2.2mm vs. HF EasyTip 2.8mm NCT01936740 | Medical University of Vienna | N/A |
| Completed | Accuracy of Holladay 2 Formula in the Absence of Lens Thickness NCT01846078 | Mahidol University | N/A |
| Completed | AcrySof® IQ ReSTOR® +2.5 D Multifocal Intraocular Lens (IOL) Model SN6AD2 [SV25T0] in Japan NCT01605877 | Alcon Research | N/A |
| Completed | Clinical Investigation of AcrySof® IQ ReSTOR® +2.5 D Multifocal Intraocular Lens (IOL) Model SN6AD2 [SV25T0] NCT01510717 | Alcon Research | N/A |
| Completed | Post Approval Study of the AcrySof® IQ Toric Intraocular Lens (IOL) Models SN6AT6-SN6AT9 NCT01601665 | Alcon Research | — |
| Completed | Comparison of Two Phacoemulsification-methods: EasyTip 2.2mm vs. Infusion Assisted EasyTip 2.2mm NCT01936727 | Medical University of Vienna | N/A |
| Completed | Randomized Comparison of the Abbott WHITESTAR Signature System With Ellips Tranversal Ultrasound vs. the Alcon NCT01279031 | Innovative Medical | Phase 4 |
| Completed | Clinical Investigation of AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric Intraocular Lens (IOL) NCT01424189 | Alcon Research | N/A |
| Completed | Clear Corneal Incisions and Arcuate Incisions Utilizing FemtoSecond Laser Technology for Cataract Surgery NCT01383057 | Innovative Medical | Phase 4 |
| Completed | Aqueous Absorption and Pharmacokinetics of Besivance Versus VIGAMOX in Patients Undergoing Phacoemulsification NCT01296191 | Frank A. Bucci, Jr., M.D. | Phase 4 |
| Completed | A Comparison of Prophylactic Antibacterial Efficacy of Besivance vs. VIGAMOX Prior to Cataract Surgery NCT01296542 | Bucci Laser Vision Institute | Phase 4 |
| Completed | AcrySof® IQ ReSTOR® +3.0 D Multifocal Toric Intraocular Lens (IOL) Clinical Study in Japan NCT01323777 | Alcon Research | N/A |
| Completed | Dispervise Ophthalmic Viscoelastic as an Agent to Ensure Watertight Wound Closure After Clear Corneal Cataract NCT01298973 | Innovative Medical | Phase 4 |
| Completed | Intra-operative Measurements to Predict the Position of the Intraocular Lens Post-operatively NCT01867541 | Prim. Prof. Dr. Oliver Findl, MBA | — |
| Unknown | Show Improved Vision With the HOYA AF-1 Aspheric Intraocular Lens After Cataract Surgery NCT01382641 | Innovative Medical | Phase 4 |
| Completed | Laser Cataract Surgery With the Femtosecond Laser Technology NCT01382823 | Innovative Medical | Phase 4 |
| Completed | Difluprednate Pediatric Study for the Treatment of Inflammation Post-Cataract Surgery NCT01124045 | Alcon Research | Phase 3 |
| Completed | An Assessment of Residual Spherical Aberration, Postoperative Total High Order Aberrations, and Functional Vis NCT01190631 | Alcon Research | N/A |
| Completed | Endothelial Cell Loss and Induced Astigmatism After Wound-directed and Wound-assisted IOL Injection NCT01250964 | University of North Carolina, Chapel Hill | N/A |
| Completed | A Comparative Pilot Study Of High-Order Aberrations With Aspheric IOL Models SN60WF and ZCB00 NCT01105585 | Alcon Research | N/A |
| Completed | Selection of Aspheric Diffractive Multifocal Intraocular Lens (IOLS) Based on Corneal Wavefront NCT00999492 | Mark Packer, MD, FACS | Phase 4 |
| Completed | A Comparison of Peak Aqueous Penetration of Acuvail (Ketorolac 0.45%), Xibrom (Bromfenac 0.09%), and Nevanac ( NCT01001806 | Frank A. Bucci, Jr., M.D. | Phase 4 |
| Completed | A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%), Xibrom (Bromfenac 0.09%)and Ne NCT01021761 | Frank A. Bucci, Jr., M.D. | Phase 4 |
| Completed | Occupational Cataracts and Lens Opacities in Interventional Cardiology : the O'CLOC Study NCT01061463 | Sophie JACOB | — |
| Terminated | Endothelial Cell Loss After Cataract Surgery NCT00932191 | University of California, San Francisco | Phase 2 / Phase 3 |
| Completed | Cataract Removal and Alzheimer's Disease NCT00921297 | University Hospitals Cleveland Medical Center | N/A |
| Withdrawn | Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Inci NCT00929747 | Alcon Research | Phase 4 |
| Terminated | Accuracy of the Galilei Analyzer to Calculate the Effective Corneal Power After Corneal Refractive Surgery NCT00934804 | Medical University of South Carolina | N/A |
| Terminated | Multifocals and Accommodating/Bilateral Implantation of Different Multifocal Intraocular Lens (IOLs) NCT00934960 | Medical University of South Carolina | — |
| Withdrawn | Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocul NCT00878839 | Alcon Research | N/A |
| Completed | Study of Difluprednate vs. Prednisolone Acetate on Visual Acuity, and Corneal Edema Following Cataract Surgery NCT01244334 | Edward J. Holland | Phase 4 |
| Completed | Safety and Effectiveness of the Calhoun Vision Light Adjustable Intraocular Lens (LAL) NCT00845520 | Calhoun Vision, Inc. | N/A |
| Completed | Visual Function Evaluation of Bilateral AcrySof ReSTOR Aspheric IOL NCT00818116 | Alcon Research | Phase 4 |
| Completed | Comparison of Tetracaine 0.5% and Lidocaine 2% Jelly for Topical Phacoemulsification Cataract Surgery NCT00827073 | Hermann Eye Center | N/A |
| Completed | Determination of Optimum Duration of Treatment With Bromfenac (Xibrom) Eyedrops Following Cataract Surgery NCT00758199 | Bp Consulting, Inc | Phase 4 |
| Completed | Comparing Optical Coherence Tomography (OCT) and Visual Acuity Outcomes in Subjects Undergoing Cataract Surger NCT00698724 | Bp Consulting, Inc | Phase 4 |
| Completed | Acrysof Toric SN60T3corneal Astigmatism Between 0.75 and 1.00 D. NCT00542581 | Medical University of South Carolina | N/A |
| Completed | AcrySof Toric Clinical Results NCT01214863 | Alcon Research | — |
| Completed | Contralateral ReSTOR / Monofocal or Phakic Eye NCT00731640 | Alcon Research | Phase 4 |
| Completed | Low Cylinder Toric NCT00732030 | Alcon Research | Phase 4 |
| Completed | DisCoVisc Comparative Evaluation NCT00732225 | Alcon Research | Phase 3 |
| Completed | Nepafenac 0.1% Eye Drops, Suspension Compared to Ketorolac Trometamol 0.5% Eye Drops, Solution and Placebo NCT00405730 | Alcon Research | Phase 3 |
| Completed | Family Studies of Eye Traits NCT00342342 | National Human Genome Research Institute (NHGRI) | — |
| Completed | Intraocular Pressure Control Following One Site Versus Two Site Combined Phacoemulsification/IOL And Trabecule NCT00695747 | Lahey Clinic | N/A |
| Completed | Modified Intraocular Lens to Reduce Eye Inflammation After Cataract Surgery in Uveitis Patients NCT00001311 | National Eye Institute (NEI) | Phase 2 |