MRI vs. surgery: study to test new way to diagnose endometriosis
NCT ID NCT06195280
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study planned to check if a specific MRI technique (3DT1) can accurately find superficial endometriosis, compared to the usual method of looking inside the belly with a camera (laparoscopy). It was designed for adults scheduled for exploratory surgery and a pelvic MRI. However, the study was withdrawn before any participants were enrolled, so no results are available.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Expected to start
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Apr 2025
An estimate. Start dates often move.
- Expected to finish
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Mar 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria : * 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. Exclusion Criteria : * Classic contraindications to magnetic resonance imaging; * Contraindications to anesthesia for exploratory laparoscopy; * Contraindication to surgery following the findings of magnetic resonance imaging results; * Patient with endometrioma \> 4 cm; * Patient with known deep endometriosis; * Patient uncooperative with protocol requirements or unable to attend the center for scheduled visits; * Pregnant woman or woman of childbearing age, without effective contraception or breastfeeding; * Patient participating in another clinical trial, or during a period of exclusion from another clinical trial; * 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; * Patient not beneficiary of a social security system * Patient under State Medical Aid.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Clinique Blomet
Paris, 75015, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can AI personalize exercise to ease pelvic pain?
- Can AI learn to spot endometriosis and fibroids on ultrasound?