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Study identifier: NCT06692335 Synced from ClinicalTrials.gov · July 28, 2026
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HIFU Versus Myomectomy for the Treatment of Symptomatic Uterine Fibroids

Condition: Uterine Fibroids (UF)  ·  Sponsor: Chinese University of Hong Kong

PhaseNA
Planned participants112
Who can joinFemale, 18 Years to 50 Years
Healthy volunteersNo

About this study

The goal of this clinical trial is to learn if High-Intensity Focused Ultrasound (HIFU) is as effective as myomectomy for treating symptomatic uterine fibroids in women aged 18 to 50. The main questions it aims to answer are: Is HIFU as effective as myomectomy in improving quality of life for women with uterine fibroids? How do the recovery times and complications compare between HIFU and myomectomy? Researchers will compare the outcomes of women receiving HIFU treatment to those undergoing myomectomy to see if HIFU offers similar or better results with fewer complications. Participants will: Undergo an initial medical assessment, including ultrasounds and blood tests. Receive either HIFU treatment or myomectomy based on random assignment. Complete questionnaires about their symptoms and quality of life before treatment and at follow-up visits (3 and 6 months post-treatment). Be monitored for any complications and recovery progress during follow-up.

This description comes directly from the study's public registry record.

Talk to the study team

Shing Chee Chan  ·  852-35052803  ·  symphorosa@cuhk.edu.hk

LAI LOI LEE  ·  852-35052583  ·  loretalee@cuhk.edu.hk

Always discuss trial participation with your own doctor first.

Locations (1)

The Chinese University of Hong KongHong Kong, Hong KongRecruiting

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Source record: clinicaltrials.gov/study/NCT06692335