UnknownNCT00390494

Questionnaire Study to Assess Quality of Life After Treatment of Fibroids

Studying Muscular tumor

Last synced from ClinicalTrials.gov April 1, 2026

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Key facts

Sponsor: U.S. Army Medical Research and Development Command
Principal Investigator: James B Spies, MD
Georgetown University Hospital
Intervention: Hysterectomy(procedure)
Enrollment: 400 target
Eligibility: 35-50 years · FEMALE
Timeline: 2005 – 2010

Study locations (4)

Georgetown University Hospital, Washington D.C., District of Columbia, United States
Walter Reed Army Medical Center, Washington D.C., District of Columbia, United States
The Cleveland Clinic Foundation, Cleveland, Ohio, United States
Magee-Womens Hospital, Pittsburgh, Pennsylvania, United States

Collaborators

Walter Reed Army Medical Center · Georgetown University · The Cleveland Clinic · University of Pittsburgh

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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