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Autologous Serum Eye Drops in Dry Eye Syndrome
Sponsor: The General Authority for Teaching Hospitals and Institutes
Summary
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.
Official title: Autologous Serum Eye Drops in Dry Eye Syndrome: Clinical Efficacy and Safety Evaluation
Key Details
Gender
All
Age Range
Any - 18 Years
Study Type
INTERVENTIONAL
Enrollment
70
Start Date
2025-09-01
Completion Date
2025-12-31
Last Updated
2025-12-22
Healthy Volunteers
No
Interventions
Autologous Serum Eye Drop
Participants will receive eye drops prepared from their blood serum following a standardized protocol. Specifically, 40 mL of venous blood was collected from each participant at the start of the study and centrifuged at 3000 rpm for 15 min.
Locations (1)
The General Authority for Teaching Hospitals and Institutes
Cairo, Egypt