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Clinical Trial Summary

The purpose of this study is to evaluate the safety and efficacy of the CyPass Implant for lowering intraocular pressure (IOP) in patients with glaucoma who undergo cataract surgery.


Clinical Trial Description

This study is a modified and expanded protocol based on acceptable safety results from an earlier feasibility study. The trial is conducted using a 3:1 randomization (treatment to control) in which patients are screened for eligibility, randomized at time of surgery and followed for 24 months postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01085357
Study type Interventional
Source Alcon Research
Contact
Status Completed
Phase N/A
Start date September 2009
Completion date March 2015

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