Evaluate the safety and efficacy of the Glaukos® Suprachoroidal Stent Model G3 in conjunction
with cataract surgery, compared to cataract surgery only, in subjects with mild to moderate
primary open-angle glaucoma.
Device: iStent supra
Procedure: Cataract surgery
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Full eligibility criteria for NCT01461278
Ages eligible for Study
45 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Mild to moderate open-angle glaucoma
Characteristics consistent with mild to moderate glaucoma
Use of one (1) to three (3) medications at time of screening exam
Pigmentary or pseudoexfoliative glaucoma
Prior incisional glaucoma surgery
All locations for NCT01461278
United States (1)
Eye Centers of Racine and Kenosha
Racine, Wisconsin, United States, 53405
View full eligibility
Tris trial is registered with FDA with number: NCT01461278. The sponsor of the trial is Glaukos Corporation and it is looking for 1200 volunteers for the current phase.
Official trial title: A Prospective, Randomized, Single-Masked, Controlled, Parallel Groups, Multicenter Clinical Investigation of the Glaukos® Suprachoroidal Stent Model G3 In Conjunction With Cataract Surgery
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