Status:

WITHDRAWN

Endometriosis: Immunomodulation

Lead Sponsor:

University of Wisconsin, Madison

Conditions:

Endometriosis

Eligibility:

FEMALE

18-45 years

Phase:

PHASE2

PHASE3

Brief Summary

The purpose of this study is to compare the effect of pioglitazone versus no drug on soluble profinflammatory markers in peritoneal fluid of women with endometriosis.

Detailed Description

The overall goal of this proposal is to assess modulation of immune mechanisms in endometriosis. Endometriosis is a common ailment affecting approximately five million reproductive-aged American women...

Eligibility Criteria

Inclusion

  • Healthy woman age 18 - 45 years.
  • Regular cycles (24-35 days).
  • Pelvic pain ≥ 3 months.
  • Negative pregnancy test.
  • Non-lactating.
  • No prior (\<3 months) use of hormonal therapy.
  • No history of liver disease.
  • Suspected endometriosis and scheduled for surgery to confirm this diagnosis
  • Surgery scheduled in follicular phase.
  • Consent to participate in the study.
  • Enrollment into data analysis portion of study if:
  • Endometriosis diagnosed from surgical specimen by routine hematoxylin and eosin staining and histological evaluation.

Exclusion

  • 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.
  • Diabetes mellitus.
  • Known pregnancy or positive pregnancy test.

Key Trial Info

Start Date :

August 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2012

Estimated Enrollment :

Patients enrolled

Trial Details

Trial ID

NCT01184144

Start Date

August 1 2010

End Date

May 1 2012

Last Update

October 2 2015

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