Actively Recruiting
Study of Pelvic Organ Mobility by Dynamic MRI in Pelvic Endometriosis
Led by University Hospital, Lille · Updated on 2025-12-26
52
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Endometriosis is a common condition affecting about 10% of women of childbearing age, and its diagnosis can be challenging due to a mismatch between symptoms and lesion severity. Researchers are investigating pelvic organ mobility in women with suspected deep pelvic endometriosis using dynamic MRI, aiming to improve diagnosis accuracy and understand treatment outcomes. This observational study focuses on how pelvic organ movement relates to symptoms and disease progression. The study evaluates a dynamic MRI sequence added to routine pelvic MRI exams. Participants include women referred for suspected pelvic endometriosis, divided into two groups based on MRI findings: those with pelvic endometriosis and those without. The dynamic MRI measures vertical displacement of pelvic organs like the vagina and cervix during rest and pushing efforts to assess mobility differences. Participants will undergo dynamic MRI scans where vertical displacement on the anterior and posterior vaginal walls and the cervix will be measured. Researchers will analyze these measurements in relation to patient symptoms and endometriosis presence. The study requires participants to be female, nulliparous, and willing to comply with procedures and follow-up. Data will help clarify pelvic organ mobility's role in endometriosis diagnosis and treatment effectiveness.
CONDITIONS
Brief Title
ENDOMETRIOSIS - MRI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient referred for suspected pelvic endometriosis requiring pelvic MRI
- Female, nulliparous
- Patient with signed written consent
- Patient with health insurance
- Patient willing to comply with all study procedures and duration
You will not qualify if you...
- Body mass index (BMI) greater than 35
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single visit
Participants undergo pelvic MRI with an additional Dynamic MRI Sequence during routine care to assess pelvic organ mobility.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Service de chirurgie gynécologique Hôpital Jeanne de Flandre - CHU de LILLE
Lille, France
Actively Recruiting
Research Team
C
Chrystele RUBOD, MD,PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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