A MULTICENTER, RANDOMIZED, DOUBLE-MASKED, SHAM-CONTROLLED, PARALLEL-GROUP PHASE 3 STUDY TO EVALUATE THE EFFICACY AND SAFETY OF EPITHELIUM-ON CORNEAL CROSS-LINKING IN SUBJECTS 8 TO 45 YEARS OF AGE WITH KERATOCONUS (APRICITY-B)
Primary Objective
To evaluate the efficacy of the riboflavin-sodium iodide solution followed by ultraviolet A (UVA) exposure and epithelium-on corneal crosslinking (CXL) assessed by visual acuity measurement in subjects with keratoconus.
Description
To evaluate the efficacy of the riboflavin-sodium iodide solution followed by ultraviolet A (UVA) exposure and epithelium-on corneal crosslinking (CXL) assessed by visual acuity measurement in subjects with keratoconus.
Details
Age
Child to Adult
Eligibility
Males and females ≥ 8 to ≤ 45 years of age with the clinical diagnosis of keratoconus. Diagnosis will be confirmed by tomographic imaging
Locations
University of Colorado Hospital
Principal Investigator
Michael Taravella
Study ID
Protocol Number: 23-1425
Categories
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