Trials / Completed
CompletedNCT03328260
High Intensity Focused Ultrasound in Uterine Myoma
Prospective, Muti-institute, Single Arm, Confirmative Trial Evaluating Efficacy and Safety of High Intensity Focused Ultrasound Device (RODIN) in Women With Symptomatic Uterine Leiomyoma
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 34 (actual)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- Female
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
Aim to evaluate the efficacy of safety of newly developed, high intensity focused ultrasound device in women with symptomatic uterine leiomyoma
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | HIFU | Transvaginal high intensity focused ultrasound to ablate uterine myoma |
Timeline
- Start date
- 2017-12-12
- Primary completion
- 2018-08-31
- Completion
- 2019-06-30
- First posted
- 2017-11-01
- Last updated
- 2020-01-03
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03328260. Inclusion in this directory is not an endorsement.