Questionnaire Study to Assess Quality of Life After Treatment of Fibroids

Status unconfirmed

Conditions studied: Leiomyoma

In brief

The purpose of this study is to determine the change in symptoms and health-related quality of life in patients undergoing treatment for fibroids. Results from the questionnaire will be compared with results obtained from patients who do not have fibroids in order to determine a score range that differentiates these two groups.

Key facts

Study ID

NCT00390494

Run by

U.S. Army Medical Research and Development Command

People needed

400

Starts

2005-12-01

Expected to finish

2010-12-01

Last updated by the study team

2008-06-30

Who can join

Age: 35 and older, up to 50. Sex: female. Healthy volunteers: accepted.

Where it is running

• 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

Full record on ClinicalTrials.gov

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