Autologous Serum Eye Drops in Dry Eye Syndrome
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 18
SponsorThe General Authority for Teaching Hospitals and Institutes
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.
Children aged less than 18 years.
Both sexes.
Diagnosed with moderate to severe dry eye syndrome (DES) refractory to artificial tears.
Active ocular infection.
Recent ocular surgery.
Systemic immunosuppressive therapy.
History of allergy to blood-derived products.