Endometriosis Pelvic Pain Interdisciplinary Cohort (EPPIC) Data Registry
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 5,000
- 试验地点
- 1
- 主要终点
- Patient-reported severity of chronic pelvic pain
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •All new and re-referred patients at the BC Women's Centre for Pelvic Pain and Endometriosis.
排除标准
- •Patients at the BC Women's Centre for Pelvic Pain and Endometriosis seen for reasons other than chronic pelvic pain and/ or endometriosis as well as patients who decline to complete the online questionnaire.
结局指标
主要结局
Patient-reported severity of chronic pelvic pain
时间窗: 3 months
Measured on a scale of 0 (no pain) to 10 (worst pain imaginable)
次要结局
未报告次要终点
研究者
Paul Yong
Research Director
BC Women's Hospital & Health Centre