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To determine the value of PET/MRI for diagnosis, therapy monitoring, and prognostic value in patients with spondyloarthritis before and after initiation of various drug therapies.

Recruiting
Conditions
M45.01 Axial spondyloarthrititis
M45.01
Registration Number
DRKS00025279
Lead Sponsor
Rheumazentrum Ruhrgebiet
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Diagnosis of spondyloarthritis (radiographic or nonradiographic axial spondyloarthritis, or psoriatic arthritis with axial skeletal involvement).
Clinical indication for [18F]fluoride PET examination.
Clinical indication for initiation of drug therapy (TNF blocker, interleuking-17 blocker, Janus kinase inhibitor, NSAID.) for a period of at least one month.

Exclusion Criteria

-Pregnancy
-Severe renal insufficiency
-Cardiac pacemaker
-Non-MR compatible foreign material
-Severe claustrophobia
-Known allergy to contrast media
-Inability to understand the patient information sheet

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To investigate the anti-inflammatory and anti-osteoblastic effects of various drug therapies (TNF blocker, interleukin-17 blocker Janus kinase inhibitor, NSAID) in patients with active spondyloarthritis during the course.<br>To investigate the correlation of clinical disease activity with the extent and course of inflammatory changes (MRI) or increased metabolic ([18F]fluoride PET) activity.
Secondary Outcome Measures
NameTimeMethod
Comparison of the examination results of native MRI examinations in the regions of the ankle, spine and sacroiliac joints of spondyloarthritis patients before and after drug therapy, among others, with the examination results obtained by means of [18F]fluoride PET/MRI. In detail, the skeletal sites showing inflammatory activity in MRI are compared to the exact anatomical regions showing metabolic activity in [18F]fluoride PET/MRI.
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