Endometriosis Trial, Recruiting NCT07053982 Sponsor: University Hospital, Toulouse Condition: Endometriosis
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Endometriosis Trial, Recruiting

NCT07053982
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:

  • You are having surgery for endometriosis and have significant pain (a pain score of 4 or higher out of 10) — this applies to the "cases" group
  • Alternatively, you are having surgery for endometriosis related to fertility problems and have little or no pain (a pain score below 4 out of 10) — this applies to the "controls" group
  • You are over 18 years old
  • You have agreed to take part and signed a consent form
  • You had an MRI scan before your surgery and there is no medical reason preventing you from having a special type of scan called an [18F]-FES PET/CT scan (confirm with trial site)
  • Your surgery took place at a specific point in your menstrual cycle (mid-cycle)
  • You are covered by a social security or health insurance scheme (confirm with trial site)

Who may not be able to join:

  • You are being treated for endometriosis without having surgery
  • You are currently pregnant
  • You are currently taking any hormone therapy
  • You have gone through menopause
  • You have a known allergy or sensitivity to the scan substance used (Fluoroestradiol (18F)) or any of its ingredients
  • You are under any form of legal guardianship or protection (confirm with trial site)
  • You experience significant anxiety in enclosed spaces (claustrophobia), which may affect your ability to have the scan

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 27 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: Ariane WEYL, MD, University Hospital, Toulouse

Phone: 05 61 32 21 48

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
Registry
ClinicalTrials.gov
Start date
23 March 2026
Est. completion
1 March 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Quantification of Estrogen Receptor Overexpression in Endometriotic Lesions Using SUV on [18F]-FES PET/CT

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: 27 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