Primary Open Angle Glaucoma (POAG) Clinical Trial
The purpose of this study is to evaluate the safety and effectiveness of CyPass implantation as a stand-alone therapy for lowering intraocular pressure (IOP) in patients with primary open angle glaucoma (POAG) who have failed at least one class of topical medical therapy
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01085357 -
Study of an Implantable Device for Lowering Intraocular Pressure in Glaucoma Patients Undergoing Cataract Surgery
|
N/A | |
| Completed |
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Safety and Performance Study of the ARGOS-IO (Intraocular) System in Patients With Primary Open Angle Glaucoma (POAG)
|
N/A | |
| Completed |
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A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS Trial
|
N/A | |
| Recruiting |
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Qlaris Phase 2 Study of QLS-111 in POAG and/or OHT Patients
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Phase 2 | |
| Completed |
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One, Two, or Three iStents for the Reduction of Intraocular Pressure in Open-angle Glaucoma Subjects
|
N/A | |
| Terminated |
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Safety Study of Latanoprost Slow Release Insert
|
Phase 1 | |
| Terminated |
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iStent Inject in OAG Subjects on 2 Pre-op Topical Ocular Hypotensive Medications
|
N/A | |
| Completed |
NCT01252849 -
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
|
N/A | |
| Active, not recruiting |
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Study to Compare Standard Perimetry With the New Scotoma-Oriented Perimetry (SCOPE) Using a New Fast German Adaptive Threshold Estimation (GATE) in Glaucoma Patients
|
N/A |