Endometriosis Trial, Recruiting NCT07397715 Sponsor: Swiss GO Trial Group Condition: Endometriosis
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Endometriosis Trial, Recruiting

NCT07397715
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Swiss GO Trial Group
Registry
ClinicalTrials.gov
Start date
15 March 2024
Est. completion
1 February 2028

Where this trial is recruiting

🇵🇱 Poland 🇪🇸 Spain 🇨🇭 Switzerland

Primary endpoints

Association between MUSA defined ultrasound features of adenomyosis and the severity of clinical symptoms.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov