Endometriosis Pelvic Pain Interdisciplinary Cohort Data Registry
Last updated on July 2021Recruitment
- Recruitment Status
- Enrolling by invitation
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Endometriosis
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Younger than 125 years
- Gender
- Only males
Description
The BC Women's Centre for Pelvic Pain and Endometriosis is the tertiary referral centre for endometriosis/pelvic pain in British Columbia, Canada. The Centre offers a unique interdisciplinary approach including minimally invasive surgery, hormonal and other medical therapy, pain education, physiothe...
The BC Women's Centre for Pelvic Pain and Endometriosis is the tertiary referral centre for endometriosis/pelvic pain in British Columbia, Canada. The Centre offers a unique interdisciplinary approach including minimally invasive surgery, hormonal and other medical therapy, pain education, physiotherapy, and CBT/mindfulness. After informed consent, patients prospectively consent to data collection in the online registry. The registry consists of patient intake questionnaires (including validated measures), physical and ultrasound examination, review of medical records, surgical findings, and annual outcomes to 5 years. The online data registry is housed in the Research Electronic Data Capture (REDCap) platform located at BC Children's Hospital.
Tracking Information
- NCT #
- NCT02911090
- Collaborators
- UBC Department of Obstetrics and Gynaecology
- Canadian Institutes of Health Research (CIHR)
- Investigators
- Principal Investigator: Paul Yong, MD PhD FRCSC BC Women's Hospital & Health Centre
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