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Efficacy of Different Treatment Regimens With Chitosan-N- Acetylcysteine in Moderate-to-severe Dry Eye Disease

Eye Diseases Clinical Trial

Official title:
Efficacy of Different Treatment Regimens With Chitosan-N- Acetylcysteine (Lacrimera®) in Moderate-to-severe Dry Eye Disease: A Pilot Study

Clinical Trial Summary

Aim of this pilot study is to evaluate the best treatment regime of Chitosan-N-Acetylcysteine (Lacrimera®) compared to preservative-free, Hyaluronic-acid containing eyedrops (Hylo-Vision® sine).

Clinical Trial Description

The present pilot study seeks to investigate the best fitting treatment regime of moderate-to-severe DED with C-NAC compared to preservative-free, Hyaluronic-acid containing eyedrops (Hylo-Vision® sine) by applying a randomized, prospective, adaptive, controlled design. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05053789
Study type Interventional
Source Vienna Institute for Research in Ocular Surgery
Contact
Status Terminated
Phase N/A
Start date May 12, 2021
Completion date August 27, 2021
View Details
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