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Clinical Trial Summary

The purpose of this study is to determine the reduction in intraocular pressure and cumulative incidence of complications between the standard and micro trabeculectomy surgeries 3 months after surgery.


Clinical Trial Description

This study is a randomized, double-masked (study participants and outcome assessors) trial. During the enrollment period, consecutive patients from LEI who are planning to have trabeculectomy surgery and who meet the study enrollment criteria will be randomized to receive standard trabeculectomy or microtrabeculectomy. The primary outcome is complications and change in intraocular pressure after a 3 month follow-up period. We will perform subgroup analyses by stratifying the population according to skin pigmentation to determine whether pigmentation is a predictor of treatment success. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02598765
Study type Interventional
Source Francis I. Proctor Foundation
Contact Jeremy D Keenan, MD, MPH
Phone 415-476-6323
Email Jeremy.Keenan@ucsf.edu
Status Recruiting
Phase N/A
Start date March 2016
Completion date March 2019

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