drugset / Trial / NCT03666884

The Comparison of 50% AS Versus PFAT+ 0.05 % COE in Severe Dry Eye Syndrome

NCT03666884

Phase 4 Completed 36 enrolled Seref istek Usak State Hospital · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The present study aimed to evaluate and compare the efficacy of a 1 month clinical trial of 50% AS for the treatment of severe dry eye syndrom (DES) based on Schirmer's Test, tear break-up time (TBUT), fluorescein staining, and ocular surface disease index (OSDI) scores, as compared to conventional preservative-free artificial tears (PFAT) plus 0.05% COE treatment in patients with severe DES

Timeline

Start
2015-10-10
Primary completion
2016-03-15
Completion
2016-10-25

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Autologous serum Unknown 50 % Topical
Comparator Cyclosporine Peptide 0.05 % Topical
Comparator Refresh Unknown

Indications