Skip to main content
Clinical Trials/NCT03002870
NCT03002870
Active, not recruiting
Not Applicable

Characteristics of Patient Population With Endometriosis - A Prospective Database and BioBank

St. Louis University1 site in 1 country2,000 target enrollmentSeptember 2016
ConditionsEndometriosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endometriosis
Sponsor
St. Louis University
Enrollment
2000
Locations
1
Primary Endpoint
Quality of life, pain and fertility
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to collect and analyze data on the characteristics of women who are seeking treatment for endometriosis, suspected endometriosis, pain and/or infertility as part of their standard medical care. Data collected will contribute to the development of guidelines for the surgical management of endometriosis. In addition, specimens will be collected for future testing regarding diagnosing, and/or staging of endometriosis, or suspected endometriosis, pain and infertility.

Detailed Description

Patients seen at Saint Louis University Center for Endometriosis (which has offices locations at St. Mary's, St. Luke's and the SLU-UMG clinic - all of which are in the SLU Epic system), and operated on for endometriosis, suspected endometriosis, pain and/or infertility at St. Mary's hospital (only). A preoperative questionnaire will be provided to the subject. Questions from the survey include information on baseline demographics, severity and type of pain, and previous medical and surgical history. Operative data will also be collected and analyzed. A post-operative questionnaire will be administered to the participants at 6 months, and then at regular yearly intervals after the surgery by a secure on-line process using the RedCap software. Improvement in quality of life and pain scores will be analyzed. Specimens will also be collected and stored for future testing regarding diagnosing, and/or staging of endometriosis, suspected endometriosis, pain and infertility.

Registry
clinicaltrials.gov
Start Date
September 2016
End Date
September 2025
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Patrick Yeung Jr., MD

Principal Investigator

St. Louis University

Eligibility Criteria

Inclusion Criteria

  • Female patients
  • 13-55 years of age
  • Anyone seen at the Center for Endometriosis

Exclusion Criteria

  • Prior bilateral salpingo-oophorectomy
  • post natural menopause
  • Significant mental or chronic systemic illness that might confound pain assessment or the inability to complete the study.

Outcomes

Primary Outcomes

Quality of life, pain and fertility

Time Frame: every 12 months

(QOL) endometriosis health profile (EHP-5)

Study Sites (1)

Loading locations...

Similar Trials