A Study of the Safety and Efficacy of Intermittent Ulipristal Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas



Status:Completed
Conditions:Women's Studies
Therapuetic Areas:Reproductive
Healthy:No
Age Range:18 - 50
Updated:11/9/2017
Start Date:January 29, 2014
End Date:January 3, 2017

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A Randomized, Placebo-Controlled, Parallel Group, Multicenter Study to Evaluate the Efficacy and Safety of Ulipristal Acetate for the Intermittent Treatment of Abnormal Uterine Bleeding Associated With Leiomyomas

This study will evaluate the superiority of ulipristal acetate vs. placebo for the treatment
of bleeding associated with uterine fibroids


Inclusion Criteria:

- Cyclic abnormal uterine bleeding (heavy or prolonged).

- Menstrual blood loss (MBL) of ≥ 80 mL in the first 8 days of menses.

- Minimum of one discrete leiomyoma observable by transvaginal ultrasound.

Exclusion Criteria:

- Evidence of malignancy or atypical or non-atypical hyperplasia on endometrial biopsy.
We found this trial at
56
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West Palm Beach, Florida
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Albuquerque, New Mexico
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Atlanta, Georgia
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Brownsburg, Indiana 46112
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Champaign, Illinois
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Charleston, South Carolina
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Clearwater, Florida
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Cleveland, Ohio
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Columbia, South Carolina
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Denver, Colorado
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Durham, North Carolina
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Englewood, Ohio
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Frisco, TX
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Granger, Indiana
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Granger, IN
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Greensboro, North Carolina
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Greenville, South Carolina 29615
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Hamilton,
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Hawaiian Gardens, California 90716
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Lawrenceville, New Jersey
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Mandeville, Louisiana 70471
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Mayfield Heights, Ohio 44124
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Metairie, Louisiana
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Miramar, Florida
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Moorestown, New Jersey 08057
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New Bern, North Carolina
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North Miami, Florida
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Orlando, Florida 32801
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Pittsburgh, Pennsylvania 15206
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Plantation, Florida
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Raleigh, North Carolina 27612
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San Antonio, Texas
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Webster, TX
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West Reading, Pennsylvania 19611
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Winston-Salem, North Carolina
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