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NCT06195280Withdrawn

SUPerficial ENDometriosis In Magnetic Resonance Imaging

Prospective, Multicenter Study Evaluating the Diagnostic Performance of the 3DT1 Sequence in Magnetic Resonance Imaging for Superficial Endometriosis

Source: ClinicalTrials.gov · Last updated 15 Jan 2026

Reason given: No patients were included in this study.

Brief summary (registry, in English)

The purpose of the study is to determine the correlation between the diagnosis of Superficial endometriosis by the 3DT1 sequence on Magnetic resonance imaging and the histology obtained by laparoscopy.

Status (registry)
Withdrawn
Study type
Interventional
Enrollment
0 (actual)
First submitted
22 Dec 2023
Start date
Apr 2025
Primary completion date
Mar 2026
Lead sponsor
GCS Ramsay Santé pour l'Enseignement et la Recherche
NCT number
NCT06195280

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindication to surgery following the findings of magnetic resonance imaging results;

Other illness

  • Patient under guardianship, under curatorship or subject to legal protection, persons deprived of liberty by a judicial or administrative decision, persons subject to psychiatric care and admitted to a health or social establishment;

Age

  • Pregnant woman or woman of childbearing age, without effective contraception or breastfeeding;

Other

  • Classic contraindications to magnetic resonance imaging;
  • Contraindications to anesthesia for exploratory laparoscopy;
  • Patient with endometrioma > 4 cm;
  • Patient with known deep endometriosis;
  • Patient uncooperative with protocol requirements or unable to attend the center for scheduled visits;
  • Patient participating in another clinical trial, or during a period of exclusion from another clinical trial;
  • Patient not beneficiary of a social security system
  • Patient under State Medical Aid.

Who the study is looking for

  • Age ≥ 18 years;
  • Non-menopausal patient;
  • Patient scheduled for exploratory laparoscopy;
  • Patient requiring a preoperative pelvic MRI
  • Patient having been informed and having signed an informed consent form.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Clinique BlometParisFranceUnknown status

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