The purpose of this study is to evaluate the efficacy, safety and duration of the L-PPDS (latanoprost punctal plug delivery system) at different dose levels.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
57
Sustained delivery for 12 weeks
Sall Research Medical Center, Inc
Artesia, California, United States
Wolstan & Goldberg Eye Associates
Los Angeles, California, United States
West Coast Eye Care Associates
San Diego, California, United States
Coastal Research Associates, LLC
Roswell, Georgia, United States
IOP change from baseline
Time frame: 12 weeks to baseline
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R and R Eye Associates
San Antonio, Texas, United States
Rocky Mountain Eye Care Associates
Salt Lake City, Utah, United States