Bone Mineral Density in Women With Uterine Fibroids or Endometriosis

NCT03744507 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 660

Last updated 2020-11-10

No results posted yet for this study

Summary

The purpose of this study is to characterize the longitudinal bone mineral density (BMD) in premenopausal women with uterine fibroids or endometriosis.

Conditions

  • Uterine Fibroid
  • Endometriosis

Sponsors & Collaborators

  • Myovant Sciences GmbH

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-03
Primary Completion
2020-07-31
Completion
2020-07-31

Countries

  • United States
  • Australia
  • Chile
  • Czechia
  • Georgia
  • Hungary
  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03744507 on ClinicalTrials.gov