Patient Centered Results for Uterine Fibroids
Completed
Conditions studied: Fibroids, Uterine
In brief
The overall goal of this project is to better enable patients with uterine fibroids (UF) to make informed decisions about treatment options by leveraging the highest possible evidence of healthcare quality. The foundation of this project will be a multi-site, prospective registry of a diverse group of women who have undergone either medical or surgical treatment for UF. Specifically, the investigators are interested in: comparing management options for symptom relief; comparing management options for preserving reproductive function; and comparing effectiveness among different subpopulations, including consideration of patient needs and preferences of treatment options.
Key facts
- Study ID
- NCT02260752
- Run by
- Duke University
- People needed
- 3094
- Starts
- 2015-11-01
- Expected to finish
- 2020-04-30
- Last updated by the study team
- 2020-11-18
Who can join
Age: 18 and older, up to 54. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of UF by imaging or pathology report within 2 years of enrollment initiation.
- Menstrual period within 12 months
You may not qualify if…
- Post-menopausal
- Men
- 55 years old or older
Where it is running
- University of California Medical Centers — San Francisco, California, United States
- Uniformed Services University of the Health Sciences — Bethesda, Maryland, United States
- Brigham and Women's Hospital — Boston, Massachusetts, United States
- University of Michigan Health System — Ann Arbor, Michigan, United States
- Henry Ford Health System — Detroit, Michigan, United States
- Mayo Clinic — Rochester, Minnesota, United States
- University of Mississippi Medical Center — Jackson, Mississippi, United States
- University of North Carolina at Chapel Hill — Chapel Hill, North Carolina, United States
- Inova Health Systems — Falls Church, Virginia, United States
Full record on ClinicalTrials.gov
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