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Completed No phase listed Observational

Bone Mineral Density in Women With Uterine Fibroids or Endometriosis

ClinicalTrials.gov ID: NCT03744507

Public ClinicalTrials.gov record NCT03744507. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 12, 2026, 3:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective Observational Study of Bone Mineral Density in Women With Uterine Fibroids or Endometriosis

Study identification

NCT ID
NCT03744507
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Myovant Sciences GmbH
Industry
Enrollment
660 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
Female
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2, 2018
Primary completion
Jul 30, 2020
Completion
Jul 30, 2020
Last update posted
Nov 9, 2020

2018 – 2020

United States locations

U.S. sites
37
U.S. states
14
U.S. cities
34
Facility City State ZIP Site status
Mobile Mobile Alabama 36608
Mesa Mesa Arizona 85215
Huntington Beach Huntington Beach California 92647
Palos Verdes Estates Palos Verdes Estates California 90274
Denver Denver Colorado 80209
United States, Colorado Denver Colorado 80211
Aventura Aventura Florida 33180
Jupiter Jupiter Florida 33458
Loxahatchee Loxahatchee Groves Florida 33470
Margate Margate Florida 33063
Miami Miami Florida 33126
Orange City Orange City Florida 32763
Orlando Orlando Florida 32835
Port St. Lucie Port Saint Lucie Florida 34952
Sarasota Sarasota Florida 34239
West Palm Beach West Palm Beach Florida 33409
Atlanta Atlanta Georgia 30328
Decatur Decatur Georgia 30034
Norcross Norcross Georgia 30093
Oak Brook Oak Brook Illinois 60523
Towson Towson Maryland 21204
Canton Canton Michigan 48187
Durham Durham North Carolina 27713
Raleigh Raleigh North Carolina 27607
Winston-Salem Winston-Salem North Carolina 27103
Columbus Columbus Ohio 43231
Chattanooga Chattanooga Tennessee 37404
Memphis Memphis Tennessee 38119
Memphis Memphis Tennessee 38120
Beaumont Beaumont Texas 77702
Fort Worth Fort Worth Texas 76104
Houston Houston Texas 77030
Houston Houston Texas 77054
San Antonio San Antonio Texas 78258
Sugar Land Sugar Land Texas 77479
Webster Webster Texas 77598
Virginia Beach Virginia Beach Virginia 23456

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03744507, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 9, 2020 · Synced May 12, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03744507 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →