A Prospective, Randomized, Single-Center, Early Feasibility Clinical Study Designed to Evaluate the Safety and Effectiveness of the GORE Glaucoma Drainage Implant (GORE GDI) in Subjects With Primary Open-Angle Glaucoma Uncontrolled by Hypotensive Medications or for Which Conventional Incisional Glaucoma Surgery Would be More Likely to Fail Due to Scarring
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- STATUS
- Recruiting
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- End date
- Apr 18, 2024
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- participants needed
- 20
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- sponsor
- W.L.Gore & Associates
Summary
The objective of this early feasibility clinical study is to evaluate the safety and effectiveness of the GORE Glaucoma Drainage Implant (2 configurations) in subjects with primary open-angle glaucoma that is uncontrolled by hypotensive medications or for which conventional incisional glaucoma surgery would be more likely to fail due to scarring.
Details
| Condition | Primary Open-angle Glaucoma |
|---|---|
| Treatment | Gore Glaucoma Device Implant (GORE GDI) |
| Clinical Study Identifier | NCT05557058 |
| Sponsor | W.L.Gore & Associates |
| Last Modified on | 18 October 2022 |
Eligibility
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