| Detected | Trial | Change |
|---|---|---|
| 2026-08-15 | NCT07036835 Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation |
date change Primary completion pushed: 2026-07 -> 2026-08 |
| 2026-08-15 | NCT07036835 Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation |
date change Completion pushed: 2026-07 -> 2026-08 |
| 2026-08-14 | NCT07228091 Surgical Procedure Efficiency Evaluation stuDy |
date change Primary completion pushed: 2026-08 -> 2027-03 |
| 2026-08-14 | NCT07228091 Surgical Procedure Efficiency Evaluation stuDy |
date change Completion pushed: 2026-08 -> 2027-03 |
| 2026-08-07 | NCT07484191 Contralateral Claims Study of Clareon Vivity Pro |
Enrollment closed, study ongoing |
| 2026-08-07 | NCT07484191 Contralateral Claims Study of Clareon Vivity Pro |
Enrollment reduced: 231 -> 165 participants |
| 2026-07-29 | NCT07238699 An Evaluation of the Safety and Tolerability of Ocular Lubricants |
Trial completed |
| 2026-07-29 | NCT07238699 An Evaluation of the Safety and Tolerability of Ocular Lubricants |
Enrollment reduced: 148 -> 124 participants |
| 2026-07-29 | NCT06285695 Clareon Toric Study (T2-T9) |
Trial completed |
| 2026-07-29 | NCT06285695 Clareon Toric Study (T2-T9) |
date change Primary completion moved earlier: 2028-07 -> 2026-06-25 |
| 2026-07-29 | NCT06285695 Clareon Toric Study (T2-T9) |
date change Completion moved earlier: 2028-07 -> 2026-06-25 |
| NCT ID | Title | Condition | Status |
|---|---|---|---|
| Phase 3 | |||
| NCT07531043 | Efficacy and Safety of FID 123472 Ophthalmic Solution for Ocular Redness in Adults | Ocular Hyperemia | Not Yet Recruiting |
| NCT07578363 | An Investigation of FID 123472 Ophthalmic Solution to Vehicle for the Reduction of Ocular… | Ocular Hyperemia | Not Yet Recruiting |
| Phase 1/2 | |||
| NCT05769153 | Study of AR-14034 in Participants With Neovascular Age-Related Macular Degeneration (nAMD) | Neovascular Age-related Macular Degeneration (nAMD) | Active, Not Recruiting |
| Not specified | |||
| NCT07147192 | Feasibility Study of an Accommodating IOL Design | Aphakia | Recruiting |
| NCT06987474 | Capella Scientia Development Study | Cataract | Recruiting |
| NCT07502456 | Clareon TruPlus Study | Aphakia | Recruiting |
| NCT07540884 | Evaluation of Tears Naturale® Free and Tears Naturale® II Lubricant Eye Drops | Dry Eye Disease | Recruiting |
| NCT04553523 | Hydrus® Microstent New Enrollment Post-Approval Study | Primary Open Angle Glaucoma | Recruiting |
| NCT07228091 | Surgical Procedure Efficiency Evaluation stuDy | Cataract | Recruiting |
| NCT05796453 | Post Market Clinical Follow-up (PMCF) Study of Clareon Vivity & Clareon PanOptix | Aphakia | Active, Not Recruiting |
| NCT05317728 | Clinical Study of a Fluid Accommodating Intraocular Lens (IOL) Design | Cataract | Active, Not Recruiting |
| NCT07161635 | Post Market Clinical Evaluation of Clareon PanOptix Pro and Clareon PanOptix Pro Toric… | Aphakia | Active, Not Recruiting |
| NCT07587138 | Clinical Evaluation of a Novel Trifocal IOL | Aphakia | Not Yet Recruiting |
| NCT07484191 | Contralateral Claims Study of Clareon Vivity Pro | Aphakia | Active, Not Recruiting |
| NCT07036835 | Clinical Investigation of a Femtosecond Laser for Corneal Flap Creation | Refractive Errors | Active, Not Recruiting |