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Clinical Trial Summary

The purpose of this study is to assess the safety and effectiveness of the Hydrus Microstent in patients with refractory open-angle glaucoma.


Clinical Trial Description

Participants will attend a screening visit, a baseline visit, a surgery visit, and 8 post-operative visits (Day 1, Day 7, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12), for a total individual duration of approximately 14 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03267134
Study type Interventional
Source Ivantis, Inc.
Contact
Status Completed
Phase N/A
Start date August 1, 2017
Completion date December 16, 2022

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