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Endometriosis Pelvic Pain Interdisciplinary Cohort Data Registry

NCT02911090 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 5000

Last updated 2024-08-07

No results posted yet for this study

Summary

The purpose of this data registry is to prospectively collect data from patients referred to an interdisciplinary clinic for pelvic pain and endometriosis to investigate long-term patient outcomes, prognosis, predictors, causes, and treatment of pelvic pain and endometriosis.

Conditions

  • Endometriosis

Interventions

OTHER

Data Registry

Data Registry

Sponsors & Collaborators

  • UBC Department of Obstetrics and Gynaecology

    collaborator UNKNOWN

  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV

  • BC Women's Hospital & Health Centre

    lead OTHER

Principal Investigators

  • Paul Yong, MD PhD FRCSC · BC Women's Hospital & Health Centre

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2028-12-31
Completion
2028-12-31

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02911090 on ClinicalTrials.gov