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Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD
Sponsor: The University of Hong Kong
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
The Thermage FLX System
The Thermage FLX System is tested for its therapeutic efficacy and safety on treating refractory Meibomian Gland Dysfunction
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