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:
- Women who are pre-menopausal or in the perimenopause stage (the years leading up to menopause) who are attending a gynaecological ultrasound appointment and agree in writing to take part.
- Women who have symptoms related to their condition, as well as women who have no symptoms.
- Women using hormonal contraceptives (such as the pill or a coil) or hormone replacement therapy (HRT) may be included, but this information will be recorded.
Who may not be able to join:
- Women who have not signed a written consent form to take part in the study.
- Women who have a serious medical, psychiatric, or psychological condition that could affect their ability to make decisions about taking part.
- Women who have already gone through menopause.
- Women who are currently pregnant.
- Women who have previously had certain pelvic or bladder surgeries, such as a TVT (a procedure for bladder leakage) or mesh surgery.
- Women who have or have had cancer or pre-cancerous changes of the womb or cervix.
- Women who have previously had surgery to remove certain types of fibroids (specifically FIGO types 3–6).
- Women who have a blood clotting disorder and are currently taking blood-thinning medication.
- Women who have been told they have internal abdominal scarring (adhesions) from a previous surgery.
- Women who have previously been diagnosed with pelvic congestion syndrome (a condition causing chronic pelvic pain related to veins in the pelvis).
- Women with a psychiatric condition that would make it difficult to accurately report pain levels.
- Women who have previously had surgery or treatment for a severe form of endometriosis called deep infiltrating endometriosis (DIE).
- Women currently experiencing urinary problems such as pain when urinating, a strong sudden urge to urinate, or significant bladder leakage.
- Women with an active or ongoing pelvic infection (such as infection of the cervix, womb lining, fallopian tubes, or a severely inflamed pelvis).
- Women with cysts or other lesions on their ovaries.
- Women who show signs of deep infiltrating endometriosis on an ultrasound scan.
- Women with certain abnormalities inside the womb cavity, such as specific types of fibroids (FIGO types 0–2), polyps, internal scarring, or retained tissue following a pregnancy.
- Women with more than 3 small fibroids (each smaller than 2 cm in size) of FIGO types 3–8 — please note that having exactly 3 fibroids smaller than 2 cm does not exclude you (confirm with trial site).
- Women who have any fibroid larger than 2 cm.
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: Gwendolin Manegold-Brauer, Prof. Dr., Deputy Head Physician, Obstetrics and Prenatal Medicine
Phone: +41612659046
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
Association between MUSA defined ultrasound features of adenomyosis and the severity of clinical symptoms.
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.