Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
52 participants
OBSERVATIONAL
2023-05-23
2026-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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patients with pelvic endometriosis
Patients referred for suspected pelvic endometriosis, with pelvic endometriosis on initial MRI
Dynamic MRI Sequence
Addition of a Dynamic MRI Sequence during the MRI examination performed in routine care
patients without pelvic endometriosis
Patients referred for suspected pelvic endometriosis but without endometriosis found on diagnostic MRI.
Dynamic MRI Sequence
Addition of a Dynamic MRI Sequence during the MRI examination performed in routine care
Interventions
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Dynamic MRI Sequence
Addition of a Dynamic MRI Sequence during the MRI examination performed in routine care
Eligibility Criteria
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Inclusion Criteria
* Female, nulliparous,
* patient with signed written consent, patient with health insurance,
* patient willing to comply with all study procedures and duration
Exclusion Criteria
* history of hereditary collagen and elastic tissue disease,
* history of pelviperitonitis,
* history of major pelvic surgery,
* inability to receive informed information,
* inability to participate in the entire study,
* lack of social security coverage,
* refusal to sign consent
18 Years
50 Years
FEMALE
No
Sponsors
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University Hospital, Lille
OTHER
Responsible Party
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Principal Investigators
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Chrystele RUBOD, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Lille
Locations
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Service de chirurgie gynécologique Hôpital Jeanne de Flandre - CHU de LILLE
Lille, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2022-A02135-38
Identifier Type: OTHER
Identifier Source: secondary_id
2022_0032
Identifier Type: -
Identifier Source: org_study_id
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