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NCT01152112 · ClinicalTrials.gov registry record · NA
HOME Study: Hysteroscopic Office Myomectomy Evaluation
A NA study, sponsored by Hologic.
- Completed
- Registry status
- NA
- Development phase
- 74
- Enrollment target
NCT01152112: Completed NA study, sponsored by Hologic.
NCT01152112 is a NA study that has completed, run by Hologic. The registered enrollment target is 74 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01152112, a NA study, has completed, sponsored by Hologic.
- COMPLETED
- Registry status
- NA
- Development phase
- 74 participants
- Enrollment target
Study Summary
The purpose of this study is to demonstrate safety and effectiveness of the MyoSure Tissue Removal System when used by community gynecologists in an office setting for the treatment of patients with symptomatic intrauterine polyps and submucosal fibroids.
Primary Outcome
Percent reduction in target pathology volume, compared between pre-treatment baseline and 3 months post MyoSure treatment
Interventions
- DEVICE Myomectomy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2010-06 |
| Est. Completion | 2013-06 |
| Phase | NA |
What the finished NCT01152112 record still lists
NCT01152112 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 1 intervention - of which Myomectomy is the first listed.
NCT01152112 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01152112 about?
NCT01152112 is a clinical study titled "HOME Study: Hysteroscopic Office Myomectomy Evaluation". The purpose of this study is to demonstrate safety and effectiveness of the MyoSure Tissue Removal System when used by community gynecologists in an office setting for the treatment of patients with symptomatic intrauterine polyps and submucosal fibroids.
What is the current status of trial NCT01152112?
This trial is currently completed. It is a NA study. The enrollment target is 74 participants. The study started on 2010-06. Estimated completion is 2013-06.
What interventions are being tested in trial NCT01152112?
The interventions under investigation include: Myomectomy (DEVICE).
Who is sponsoring clinical trial NCT01152112?
This trial is sponsored by Hologic, which has 21 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01152112's enrollment target sits among peer trials
74 1082nd of 2000 higher than 912 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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