U.S., April 15 -- ClinicalTrials.gov registry received information related to the study (NCT07529899) titled 'A Prospective, Multicenter, Randomized Controlled Trial to Evaluate the Efficacy and Safety of Amnion Membrane Disc Allograft Versus Standard of Care in Participants With Moderate to Severe Dry Eye Disease' on April 08.
Brief Summary: To evaluate the efficacy of Lyophilized Human Amnion Membrane Disc in reducing corneal epithelial damage as measured by the Lexitas Modified National Eye Institute (NEI) Grading Scale for Corneal Fluorescein Staining.
Study Start Date: July, 2026
Study Type: INTERVENTIONAL
Condition:
Dry Eye Disease (DED)
Intervention:
PROCEDURE: Standard of Care (SOC)
Standard of care is to perform eye cleansi...