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Autologous Serum Eye Drops in Dry Eye Syndrome: Clinical Efficacy and Safety Evaluation
This study aims to evaluate the clinical efficacy and safety of autologous serum eye drops (ASEDs) in patients with moderate-to-severe dry eye syndrome who are refractory to conventional artificial tear therapy.
Dry Eye Syndrome (DES) is a highly prevalent ocular condition that significantly affects quality of life, with global prevalence estimated at 5%-50%, depending on population and diagnostic criteria. Autologous Serum Eye Drops (ASEDs) have emerged as a promising therapy due to their composition, which is rich in vitamin A, epidermal growth factor, fibronectin, and transforming growth factor-β. These components mimic natural tears and promote epithelial healing, reduce inflammation, and enhance tear film stability.
Age
0 - 18 years
Sex
ALL
Healthy Volunteers
No
The General Authority for Teaching Hospitals and Institutes
Cairo, Egypt
Start Date
September 1, 2025
Primary Completion Date
December 31, 2025
Completion Date
December 31, 2025
Last Updated
December 22, 2025
70
ESTIMATED participants
Autologous Serum Eye Drop
OTHER
Lead Sponsor
The General Authority for Teaching Hospitals and Institutes
Data Source & Attribution
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