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Clinical Trial Summary

This is a prospective, non-randomized, single-arm early feasibility study to assess the safety and feasibility of lowering intraocular pressure with the Brown Glaucoma Implant. A total of up to 10 subjects will be enrolled at three centers. Subjects will be followed for 24 months, with the primary assessments completed 6 months after implant.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03469297
Study type Interventional
Source MicroOptx
Contact
Status Completed
Phase N/A
Start date May 1, 2018
Completion date September 20, 2021

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