Trials / Completed
CompletedNCT01252849
Purpose of This Study is to Evaluate the Safety and Efficacy of One, Two, or Three iStents for the Reduction of Intraocular Pressure in Open-angle Glaucoma Subjects
A Prospective, Randomized, Controlled Evaluation of Open-Angle Glaucoma Subjects on Two Topical Hypotensive Medications, Implanted With One, Two, or Three Trabecular Micro-Bypass Stents
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 119 (actual)
- Sponsor
- Glaukos Corporation · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the safety and efficacy of the iStent medical device that is implanted into the eye and designed to reduce eye pressure in patients with your condition.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | iStent | Implantation of One iStent through a small temporal clear corneal incision. |
| DEVICE | iStent | Implantation of Two iStents through a small temporal clear corneal incision |
| DEVICE | iStent | Implantation of Three iStents through a small temperal clear corneal incision |
Timeline
- Start date
- 2010-12-01
- Primary completion
- 2019-10-08
- Completion
- 2019-10-08
- First posted
- 2010-12-03
- Last updated
- 2022-08-31
Locations
1 site across 1 country: Armenia
Source: ClinicalTrials.gov record NCT01252849. Inclusion in this directory is not an endorsement.