Post Approval Study of the CyPass System

Status Terminated

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

Clinical Trial Details

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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