NL-OMON39151
Completed
Not Applicable
Sensitive Imaging in Ankylosing Spondylitis - SIAS
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Ankylosing Spondylitis
- Sponsor
- eids Universitair Medisch Centrum
- Enrollment
- 40
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a) Male and female patients of at least 18 years having Ankylosing Spondylitis (AS) fulfilling the Modified New York criteria, in which a patient has \*definite\* AS if the radiological criterion is associated with at least one clinical criterion: ;Clinical criterions:
- •\* low back pain and stiffness for more than 3 months that improves with exercise, but is not relieved by rest.
- •\* limitation of motion of the lumbar spine in the sagittal and frontal planes.
- •\* limitation of chest expansion relative to normal values correlated for age and sex.;Radiological criterion (sacroiliitis grade \>\= 2 bilaterally or grade 3\-4 unilaterally)
- •\* grade 0 \= no sacroiliitis
- •\* grade 1 \= blurring of the joint margins (\*suspicious\*)
- •\* grade 2 \= sclerosis, erosions, no changes in joint space
- •\* grade 3 \= erosions, changes in joint space, partial ankylosis
- •\* grade 4 \= complete ankylosis;b) Patients should have at least one syndesmophyte in either the cervical or lumbar spine radiograph at baseline conventional radiography. The maximum number of VUs is 9 (out of 12\). ;c) The patient should have given written informed consent.
Exclusion Criteria
- •\* \> 9 by syndesmophytes affected vertebral units.;\* A history of alcoholism, drug abuse, psychological or other emotional problems, severe comorbidity likely to invalidate informed consent or limit the ability of the subject to comply with the protocol requirements.;\* Routine MRI\-contraindications (e.g. instable metal implants, pacemaker/ICD, vascular clips, hearing aids and claustrophobia).;\* Pregnancy.
Outcomes
Primary Outcomes
Not specified
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