Expired Study
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San Antonio, Texas


Purpose:

This study will evaluate the degree of post-operative ocular inflammation in patients who are undergoing a pars plana vitrectomy.


Criteria:

Inclusion Criteria: - Require pars plana vitrectomy in at least 1 eye - Best corrected visual acuity in the study eye between 20/400 and 20/40 Exclusion Criteria: - Use of any NSAIDs (topical or systemic) within 14 days - Use of topical or systemic steroids within 30 days - Active eye infection in either eye - Any eye surgery within 6 months - Prior pars plana vitrectomy, YAG capsulotomy or uveitis


NCT ID:

NCT01319318


Primary Contact:

Study Director
Medical Director
Allergan


Backup Contact:

N/A


Location Contact:

San Antonio, Texas
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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