Spots Global Cancer Trial Database for High Intensity Focused Ultrasound in Uterine Myoma
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Trial Identification
Brief Title: High Intensity Focused Ultrasound in Uterine Myoma
Official Title: Prospective, Muti-institute, Single Arm, Confirmative Trial Evaluating Efficacy and Safety of High Intensity Focused Ultrasound Device (RODIN) in Women With Symptomatic Uterine Leiomyoma
Study ID: NCT03328260
Conditions
Interventions
Study Description
Brief Summary: Aim to evaluate the efficacy of safety of newly developed, high intensity focused ultrasound device in women with symptomatic uterine leiomyoma
Detailed Description:
Keywords
Eligibility
Minimum Age: 19 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Locations
Seoul National University Bundang Hospital, Seongnam Si, Gyenggi DO, Korea, Republic of
Contact Details
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