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NCT00194233 Clinical Trial

Serum and Peritoneal Fluid Bank for Endometriosis Markers

Endometriosis Clinical Trial

Official title:
Serum and Peritoneal Fluid Bank for Assessment of Markers of Endometriosis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00194233
Other study ID # 708870
Secondary ID RRU008
Status Completed
Phase N/A
First received September 13, 2005
Last updated August 15, 2016
Start date November 2003
Est. completion date June 2008

Study information
Verified date August 2016
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate differences in protein expression profiles of blood and peritoneal fluid samples obtained from patients who do, and those who do not, have endometriosis seen during laparoscopic surgery. These profiles may include both known and novel markers for diagnosing endometriosis.

Recruitment information / eligibility
Status Completed
Enrollment 300
Est. completion date June 2008
Est. primary completion date January 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Undergoing laparoscopic surgery for one of the following indications:

1. infertility

2. pain

3. tubal sterilization

- For cases, visualization of endometriosis

- For controls, absence of endometriosis

Exclusion Criteria:

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States University of Pennsylvania Reproductive Research Unit Philadelphia Pennsylvania

Sponsors (1)
Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

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