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Intense Regulated Pulsed Light Vs Standard of Care for the Treatment of Meibomian Gland Dysfunction

Meibomian Gland Dysfunction Clinical Trial

Official title:
Intense Regulated Pulsed Light Vs Standard of Care for the Treatment of Meibomian Gland Dysfunction

Clinical Trial Summary

This study is to evaluate the effectiveness of E>EYE intense regulated pulsed light (IRPL) treatment compared to the current standard of care using a daily warm compress

Clinical Trial Description

E-Eye is a medical device that has been specifically designed for treating dry eye syndrome due to meibomian gland dysfunction (MGD). This study is a prospective, single centred, interventional, randomized study assessing the efficacy and safety of E>EYE in the management of MGD (3 applications on days 0, 15 and 45, with a follow up 1 month later) compared to daily use of a warm compress over a period of 75 days. The study will monitor the change in symptoms and signs of dry eye at each visit.) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04920396
Study type Interventional
Source Aston University
Contact
Status Suspended
Phase N/A
Start date June 8, 2021
Completion date December 16, 2026
View Details
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