Treatment of Endometrial Hyperplasia With an Intrauterine Device (IUD)

Status Withdrawn

Clinical Trial Summary

The purpose of this research is to determine the effectiveness of the intrauterine device (IUD) called Mirena when compared to the Provera tablets used in treating this condition.

Clinical Trial Description

Endometrial hyperplasia without atypia is a condition usually caused by excessive stimulation of the uterine lining (endometrium) by estrogens, and may cause irregular bleeding as a presenting symptom, but rarely may progress to endometrial cancer, which makes treatment important. The only treatment approved so far is medroxyprogesterone acetate tablets (progesterone), also known as Provera. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00123175
Study type	Interventional
Source	Milton S. Hershey Medical Center
Contact
Status	Withdrawn
Phase	Phase 1/Phase 2
Start date	September 2009
Completion date	September 2011

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