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RECRUITING
NCT06220474
NA

Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD

Sponsor: The University of Hong Kong

View on ClinicalTrials.gov

Summary

The goal of this prospective, 24-week, double-masked, randomized, sham-controlled clinical trials to compare clinical efficacy and safety of RF and MGX with MGX alone in patients with meibomian gland dysfunction-related dry eye disease. The main question it aims to answer is whether radiofrequency treatment and meibomian gland expression is more effective in improving tear breakup time, as measured using non-invasive video keratography, compared with meibomian gland expression alone, in patients with refractory meibomian gland dysfunction-related dry eye disease. Participants will be divided into two groups, one group will receive RF treatment followed with MGX and another will receive sham treatment with MGX.

Official title: Therapeutic Efficacy and Safety of Non-Invasive Radiofrequency Treatment in Patients With Refractory Meibomian Gland Dysfunction: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

112

Start Date

2024-10-22

Completion Date

2027-12-31

Last Updated

2024-12-02

Healthy Volunteers

No

Interventions

DEVICE

The Thermage FLX System

The Thermage FLX System is tested for its therapeutic efficacy and safety on treating refractory Meibomian Gland Dysfunction

DEVICE

Sham treatment

Sham treatment acts as a control to test the therapeutic efficacy and safety of The Thermage FLX System

Locations (2)

Grantham Hospital

Hong Kong, Hong Kong

HKU Eye Centre

Hong Kong, Hong Kong