Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD
NCT: NCT06220474 · RECRUITING
Brief 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.
Frequently Asked Questions
What is Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD?
Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD is a clinical trial registered under NCT06220474. Current status: RECRUITING.
What is the status of NCT06220474?
The current status of NCT06220474 (Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD) is: RECRUITING.
When did Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD start?
Therapeutic Efficacy and Safety of Non-Invasive RF Treatment in Refractory MGD started on 2024-10-22.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.