PrePOSE

  • Research type

    Research Study

  • Full title

    Predicting the Pain Outcome of Surgery for Endometriosis (PrePOSE)

  • IRAS ID

    349041

  • Contact name

    Katy Vincent

  • Contact email

    katy.vincent@wrh.ox.ac.uk

  • Sponsor organisation

    University of Oxford / Research Governance, Ethics and Assurance

  • Clinicaltrials.gov Identifier

    NCT07313345

  • Duration of Study in the UK

    3 years, 0 months, 1 days

  • Research summary

    Endometriosis is a chronic gynaecological condition that affects around 10% of women of reproductive age. This condition can cause debilitating pain, infertility, and poor quality of life. Endometriosis is a condition where endometrial-like tissue is present outside of the uterus which can cause inflammation around the pelvic area. Symptoms of endometriosis can consist of pain during the menstrual cycle, chronic pelvic pain, pain during sex, pain when urinating, pain when defecating, and fatigue. Current treatments for endometriosis consist of hormonal, anti-inflammatory and / or analgesic medications and laparoscopic surgery. Endometriosis is categorized into 4 stages (I – IV), with surgery often being the treatment suggestion for patients with stages III and IV. However, laparoscopic surgery does not always result in a reduction in pain for patients with endometriosis, therefore, it is important to try and understand which patients are most likely to benefit from surgery for their pain management. In the present study, patients with pelvic endometriosis at stage III or IV with planned surgical treatment scheduled will be recruited to the project. Participants taking part will provide data at 5 different time points: Time point 1 will consist of several baseline questionnaires, a physiological pain assessment, and a brain functional magnetic resonance imaging (fMRI) scan. Time point 2 will be the date of their endometriosis surgery, where a questionnaire will be taken, the surgery will be completed, and several biological samples will be taken. Time points 3 (3 months post-surgery), 4 (6 months post-surgery), and 5 (12 months post-surgery) will consist of completing online questionnaires. All data collected within this project will be used to investigate pain outcome following endometriosis surgery. This research is funded by NIHR BRC.

  • REC name

    South East Scotland REC 02

  • REC reference

    25/SS/0062

  • Date of REC Opinion

    30 Sep 2025

  • REC opinion

    Further Information Favourable Opinion