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Incidence of MRI Sacro-Iliac Joint Anomalies in Young Women (MISIA)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Completed

Conditions

Women (Between 18 to 50 Years Old)
Inflammatory Lesions
Structural Lesions
Axial Spondyloarthritis
Sacro-iliac Joints

Treatments

Other: Standard care

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Prospective multicenter study assessing the incidence of inflammatory and structural lesions seen on MRI of the SI joints in a consecutive population of women aged 18-50 years old.

The study hypothesis is SpA may be misdiagnosed on MRI in post partum women due to increased stress on the joint following pregnancy and childbirth, as MRI of the SI joints may show lesions that could mimics axial spondyloarthritis. The primary objective of this study is to determine the incidence of SI lesions seen at MRI in women. The secondary objectives are to compare the incidence and pattern of MRI inflammatory and structural lesions of the SI joints and to determine the factors associated with inflammatory or structural changes of the SI joints in a population of women. the investigators will especially compare the population of women within a year after childbirth versus the population of women who never gave birth or who gave birth over 24 months ago or more.

Full description

500 women aged of 18 to 50 years old, including 100 women who gave birth within the year, referred to the Imaging department for pelvic MRI for the exploration of pelvic or gynecologic pathology will be recruited consecutively.

MRI will be performed on a 1.5 T MRI according to standardized exploration of the pelvis and will include axial T1-weighted sequences and T2STIR (or T2 fat sat or T2 Dixon) of maximum 6 mm thickness .

An additional Axial STIR sequence may be added as part of the research (duration 3 minutes), if the standard protocol does not include any STIR, T2 fat sat T2 or T2 Dixon sequence.

SI lesions will be assessed in a centralized randomized and independent review of all MR images by 2 musculoskeletal radiologists according to ASAS criteria.

Patients will complete a standardized questionnaire on the day of MRI to collect the following data : patient's and family history of chronic inflammatory disease, number and date of pregnancies, practice of sports, back pain, joint pain.

Enrollment

512 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women aged 18 to 50 years old
  • MRI of the pelvis requested as part of an exploration of a gynecological or pelvic pathology
  • Women who delivered within the year OR women who never gave birth or gave birth 24 months ago and over

Exclusion criteria

  • Patients with a personal or family history of inflammatory disease (SpA , ulcerative colitis , chron , PSO , RA, SAPHO)
  • Patients with a history of trauma or surgery of the pelvis
  • Pregnant women
  • Women who gave birth over a year ago and less than 2 years ago

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Central trial contact

Catherine CYTEVAL, PU-PH

Data sourced from clinicaltrials.gov

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