Overview

Use of Rosiglitazone in the Treatment of Endometriosis

Status:
Terminated
Trial end date:
2006-05-01
Target enrollment:
0
Participant gender:
Female
Summary
The purpose of this study is to perform a pilot study on the efficacy of rosiglitazone in reducing pelvic pain in early stage endometriosis patients.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Collaborator:
Berlex Foundation
Treatments:
Rosiglitazone
Criteria
Inclusion Criteria:

- Healthy women ages 18 - 45 years.

- Regular menstrual cycles (24-35 days).

- Pelvic pain ≥ 3 months with cyclical component.

- Negative pregnancy test and must use nonhormonal contraception.

- Non-lactating.

- No history of liver disease.

- Consent to participate in the study.

- Endometriosis diagnosed from surgical specimen by routine hematoxylin and eosin
staining and histological evaluation within the past 4 years.

Exclusion Criteria:

- Major psychiatric conditions or the abuse of alcohol or drugs which would make it
difficult for the subject to complete study procedures.

- Active or prior infection with hepatitis, human immunodeficiency virus (HIV)
infection, or history of high-risk activities (e.g., IV drug abuse) which would
increase risk to laboratory personnel. Of note, no testing for hepatitis or HIV will
be performed as part of this study and all tissues will be handled and discarded as if
they were potentially infected.

- Patients with liver dysfunction (elevated liver enzymes > 2 times the upper limit of
normal).

- Presence of pre-existing malignancy, including carcinoma of the breast or uterus.

- Women with other causes of chronic pelvic pain including infectious, gastrointestinal,
musculoskeletal, neurologic or psychiatric.

- Elevated WBC.

- NYHA functional class I-IV heart failure.

- Diabetics.

- Known pregnancy or positive pregnancy test.