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

Recruiting N/A Interventional Study
Dry Eye Syndromes Meibomian Gland Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
112 (estimated)
Sponsor
The University of Hong Kong · Other
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About This Trial
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 measure…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Age 18 or more 2. Bilateral dry eye disease as confirmed by presence of both symptoms and signs 2.1 Symptoms: Abnormal result on the Standard Patient Evaluation of Eye Dryness Questionnaire (SPEED) dry eye symptom questionnaire (≥5) 2.2 Signs: Abnormal result in at least one …
Contacts

Kendrick Co SHIH

94326271

kcshih@hku.hk

CONTACT