Phase 4 Endometrial Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have uterine fibroids (non-cancerous growths in the womb) that need to be surgically removed, while keeping your uterus intact
- You are willing and able to follow all the study's requirements for the full length of the trial
- You are able to sign and date a consent form agreeing to take part
Who may not be able to join:
- You have already been diagnosed with anxiety or depression
- You have a pre-existing condition that affects how your blood clots (confirm with trial site)
- You already experience nerve pain or long-term ongoing pelvic pain
- You regularly use opioid pain medicines (such as morphine or codeine) on an ongoing basis
- You are unable to read and understand straightforward written questionnaires
- You do not speak English
- Your Body Mass Index (BMI), which is a measure of body weight relative to height, is higher than 38
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Joseph Findley, MD, University Hospitals
Phone: 3392011531
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Time in minutes from first analgesic request as measured by medical chart review; Total number of doses of rescue analgesics given as measured by medical chart review
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.