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Clinical Trial Summary

Objective : To demonstrate diagnostic performances of Magnetic Resonance Imaging (MRI) as compared to Computed Tomography (CT) as a second intention imaging modality in young women with acute non traumatic abdominopelvic pain and non contributive ultrasonography.


Clinical Trial Description

Methods : Consecutive women aged 18-40 years old with acute abdominopelvic pain referred to CT by the emergency Physician or gynaecologist after a non contributive ultrasonography will be included. After obtaining informed consent, all patients will undergo standard CT followed by an additional MRI examination, performed using a short MRI protocol and within 6 hour from CT. The gold standard or reference diagnosis will be established in consensus by an expert panel at 3 months follow up using a standardized diagnosis form. A retrospective reading will be performed independently for CT and MRI by radiologists blinded to the reference diagnosis, using the same standardized diagnosis form. CT and MRI accuracies will be compared. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03281031
Study type Interventional
Source University Hospital, Montpellier
Contact Ingrid MILLET, MD, PhD
Phone 0467338817
Email i-millet@chu-montpellier.fr
Status Recruiting
Phase N/A
Start date October 18, 2017
Completion date October 2022

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