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Clinical Trial Summary

The purpose of this study is to demonstrate that the rate of clinically relevant complications associated with CyPass Micro-Stent placement and stability using the CyPass 241-S applier, as determined at 36 months in the postmarket setting, is less than the pre-specified performance target, which is based on experience with the CyPass Model E applier in COMPASS trial TMI-09-01 (NCT01085357).


Clinical Trial Description

Each subject's expected participation in the study is up to 37.5 months which includes up to 42 days between the screening and surgery visits, and 36 months of post-surgery follow-up. Only one eye per subject will be implanted. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03273907
Study type Interventional
Source Alcon Research
Contact
Status Terminated
Phase N/A
Start date October 12, 2017
Completion date August 31, 2021

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