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

  • End date
    Apr 18, 2024
  • participants needed
  • sponsor
    W.L.Gore & Associates
Updated on 18 October 2022
glaucoma surgery
Accepts healthy volunteers


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.

Condition Primary Open-angle Glaucoma
Treatment Gore Glaucoma Device Implant (GORE GDI)
Clinical Study IdentifierNCT05557058
SponsorW.L.Gore & Associates
Last Modified on18 October 2022


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