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NCT03744507 · ClinicalTrials.gov registry record
Bone Mineral Density in Women With Uterine Fibroids or Endometriosis
A clinical trial, sponsored by Myovant Sciences.
- Completed
- Registry status
- 660
- Enrollment target
NCT03744507 is a clinical trial that has completed, run by Myovant Sciences. The registered enrollment target is 660 participants.
The verdict
NCT03744507 has completed, sponsored by Myovant Sciences.
- COMPLETED
- Registry status
- 660 participants
- Enrollment target
Study Summary
The purpose of this study is to characterize the longitudinal bone mineral density (BMD) in premenopausal women with uterine fibroids or endometriosis.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 660 participants |
| Start Date | 2018-08-03 |
| Est. Completion | 2020-07-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03744507
The ClinicalTrials.gov registry entry for NCT03744507 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 660 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Myovant Sciences, which has 11 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 0 interventions.
NCT03744507 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03744507 about?
NCT03744507 is a clinical study titled "Bone Mineral Density in Women With Uterine Fibroids or Endometriosis". The purpose of this study is to characterize the longitudinal bone mineral density (BMD) in premenopausal women with uterine fibroids or endometriosis.
What is the current status of trial NCT03744507?
This trial is currently completed. The enrollment target is 660 participants. The study started on 2018-08-03. Estimated completion is 2020-07-31.
Who is sponsoring clinical trial NCT03744507?
This trial is sponsored by Myovant Sciences, which has 11 total clinical trials registered on ClinicalTrials.gov.
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