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Clinical Trial Summary

Adult subjects with elevated intraocular pressure who have successfully undergone placement of iStent infinite trabecular bypass system will be randomized to receive a travoprost intraocular implant or receive a sham procedure and be followed for 12 months.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06066645
Study type Interventional
Source Glaukos Corporation
Contact Study Director
Phone 949-481-8076
Email idose@glaukos.com
Status Recruiting
Phase Phase 3
Start date September 14, 2023
Completion date November 2025

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