Multicenter Post-Approval Study Of The Glaukos® iStent® Trabecular Micro-Bypass Stent System In Conjunction With Cataract Surgery
Status: | Active, not recruiting |
---|---|
Conditions: | Ocular, Ocular |
Therapuetic Areas: | Ophthalmology |
Healthy: | No |
Age Range: | 22 - Any |
Updated: | 8/2/2018 |
Start Date: | July 2013 |
End Date: | July 2021 |
A Prospective, Controlled, Multicenter Post-Approval Study Of The Glaukos® iStent® Trabecular Micro-Bypass Stent System In Conjunction With Cataract Surgery
The purpose of this study is to assess the long-term safety of the Glaukos® iStent®
Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery vs. cataract
surgery only, in subjects with mild to moderate open-angle glaucoma.
Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery vs. cataract
surgery only, in subjects with mild to moderate open-angle glaucoma.
The purpose of this study is to assess the long-term safety of the Glaukos® iStent®
Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery compared to
cataract surgery only, in subjects with mild to moderate open-angle glaucoma.
Trabecular Micro-Bypass Stent Model GTS100 in conjunction with cataract surgery compared to
cataract surgery only, in subjects with mild to moderate open-angle glaucoma.
Inclusion Criteria:
- mild to moderate primary open-angle glaucoma
- currently treated with ocular hypotensive medication
- pseudoexfoliative and pigmentary glaucoma are acceptable diagnoses
- subject scheduled to undergo cataract surgery
Exclusion Criteria:
- primary angle-closure glaucoma; or secondary angle closure glaucoma, including
neovascular glaucoma
- retrobulbar tumor, thyroid eye disease, Sturge-Weber syndrome or any other type of
condition that may cause elevated episcleral venous pressure
We found this trial at
15
sites
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Winston-Salem, North Carolina
Phone: 949-367-9600
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