The primary focus of this study is to assess intraocular pressure and complication rates between patients who receive mitomycin-C using a sponge versus no-sponge.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
100
Duke University Medical Center
Durham, North Carolina, United States
Complication Rates
To assess complication rates between patients who receive mitomycin-C using a sponge versus irrigation
Time frame: post-operative day 1 to month 6
Change in Intraocular Pressure
To assess final intraocular pressure lowering between patients who receive mitomycin-C using a sponge versus irrigation
Time frame: post-operative day 1 to month 6
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