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Completed

NCT Number: NCT00881140

Efficacy Study of Vaginal Mifepristone to Treat Uterine Fibroids

The purpose of this study is to evaluate the effect of daily dosage of vaginally mifepristone on reduction of uterine fibroids size and the symptoms associated with uterine fibroids.

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Key information

About this study

Uterine fibroids are benign tumors of the uterus made up of smooth muscle and the extracellular matrix proteins Collagen and Elastin. They are exceptionally common; the cumulative incidence of a diagnosis of fibroids in women aged 25 to 45 is approximately 30 percent.

Uterine fibroids can cause abnormal uterine bleeding, dysmenorrhea, lower back pain and non-cyclic pelvic pain. They also can contribute to symptoms related to an enlarging pelvic mass (e.g., urinary frequency or constipation).

Uterine fibroids are also associated with an increased risk of complications of pregnancy, and with infertility, although it is unclear whether this association is causative. Symptoms associated with uterine fibroids can have a significant impact on quality of life, with scores on standard measures that are comparable to those for other major chronic diseases

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Uninterested in fertility during the study.
  • Premenopausal status.
  • Active symptoms related to uterine fibroids.
  • Subjects will be obligated to use non hormonal contraceptives during the study.

Exclusion criteria

  • Abnormal liver and renal function
  • Participants with significant increase in uterine fibroids size during a short time.
  • Exclusionary health problems contraindicating mifepristone included adrenal disease; sickle cell anemia; severe liver, respiratory, or renal disease; and blood clotting defect.
  • Current use of steroids, anticoagulants, herbals, or botanicals with possible hormonal effects.

Treatment and study plan

mifepristone vaginal tablets

Drug

Daily use of 10 mg administrated per vagina for 3 months

Other names: mifepristone

Primary outcomes

  1. Decrease of uterine fibroids volume by 25% and up.

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

BioPro Medical Ltd

Industry

Registry information

Official study title

The Effect of Vaginal Mifepristone on Reduction of Uterine Fibroids Size and the Symptoms Associated With the Fibroids - Pilot Study (Phase IIa)

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Apr 15, 2009
Registry last updated
Dec 19, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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