Endometriosis 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 are willing and able to sign a written consent form agreeing to take part.
- You are a female between 14 and 50 years old at the time of signing the consent form.
- You are already scheduled to have open or keyhole surgery because your symptoms suggest you may have endometriosis.
Who may not be able to join:
- You have not yet had your first menstrual period.
- You are currently pregnant.
- You currently have an active cancer diagnosis.
- You have previously tested positive for HIV or hepatitis A, B, or C.
- You currently have an active infection in your pelvis or any other infection that would make surgery unsafe.
- You have taken part in another clinical trial involving an experimental drug, device, or procedure within 3 months before joining, or have one planned within 3 months of joining.
- You have a general health or behavioural condition that the trial doctor believes would make it unsuitable for you to participate (confirm with trial site).
- You are under 14 or over 50 years old.
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: Todd Pappas, PhD, Aspira Women's Health
Phone: 844-277-4721
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
Sensitivity and Specificity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.