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Efficacy of Two Concentrations of Autologous Serum for the Treatment of Severe Dry Eye

Dry Eye Clinical Trial

Official title:
Comparison of Autologous Serum 20% and Autologous Serum 50% for the Treatment of Severe Dry Eye

Clinical Trial Summary

The purpose of this study is to compare the effects of autologous serum 20% and autologous serum 50% for the treatment of Severe Dry Eye Syndrome

Clinical Trial Description

To determine the difference between autologous serum 20% vs 50%, in terms of improvement of symptoms, improvement of ocular surface parameters and acceptable tolerability in patients with severe dry eye syndrome. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03436576
Study type Interventional
Source Pontificia Universidad Catolica de Chile
Contact
Status Enrolling by invitation
Phase Phase 3
Start date September 12, 2018
Completion date November 19, 2018
View Details
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