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NCT00131365 · ClinicalTrials.gov registry record · NA
Magnetic Resonance (MR) Guided Focused Ultrasound Surgery of Uterine Fibroids
A NA study, sponsored by InSightec.
- Completed
- Registry status
- NA
- Development phase
- 9
- Enrollment target
NCT00131365 is a NA study that has completed, run by InSightec. The registered enrollment target is 9 participants.
The verdict
NCT00131365, a NA study, has completed, sponsored by InSightec.
- COMPLETED
- Registry status
- NA
- Development phase
- 9 participants
- Enrollment target
Study Summary
The goal of this study is to develop additional long term data to evaluate the safety and effectiveness of this treatment. Indications for use for this system is: 'The ExAblate is intended to ablate uterine fibroid tissue in pre- or peri-menopausal women with symptomatic uterine fibroids who desire a uterine sparing procedure. Patients must have a uterine size of less than 24 weeks and not seeking treatment for reasons of improving fertility.'
Interventions
- DEVICE ExAblate 2000
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9 participants |
| Start Date | 2006-01 |
| Est. Completion | 2009-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00131365
The ClinicalTrials.gov registry entry for NCT00131365 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 9 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InSightec, which has 38 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which ExAblate 2000 is the first listed.
NCT00131365 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00131365 about?
NCT00131365 is a clinical study titled "Magnetic Resonance (MR) Guided Focused Ultrasound Surgery of Uterine Fibroids". The goal of this study is to develop additional long term data to evaluate the safety and effectiveness of this treatment. Indications for use for this system is: 'The ExAblate is intended to ablate uterine fibroid tissue in pre- or peri-menopausal women with symptomatic uterine fibroids who desire...
What is the current status of trial NCT00131365?
This trial is currently completed. It is a NA study. The enrollment target is 9 participants. The study started on 2006-01. Estimated completion is 2009-02.
What interventions are being tested in trial NCT00131365?
The interventions under investigation include: ExAblate 2000 (DEVICE).
Who is sponsoring clinical trial NCT00131365?
This trial is sponsored by InSightec, which has 38 total clinical trials registered on ClinicalTrials.gov.
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