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Clinical Trial Summary

This is prospective, non-randomized, single-arm study to assess the safety and effectiveness of lowering intraocular pressure with the Beacon Aqueous Microshunt. A total of 65 subjects will be enrolled at five centers. The primary endpoint will be assessed at 12 month follow-up.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03634319
Study type Interventional
Source MicroOptx
Contact
Status Terminated
Phase N/A
Start date June 1, 2018
Completion date January 8, 2023

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