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Starting soon Observational

Severity Over Time of Early Forms of Spondyloarthritis

NCT06261931 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-02-12
Last updated
2024-02-15

Condition(s) studied

SpondyloarthritisSpondyloarthritis, Axial

Investigational drug(s) / intervention(s)

Diagnostic assessmentDiagnostic assessment

Diagnostic assessment: patient with sponiloarthritis who comes to the clinic Hospital for clinical evaluation of disease. Assessment instrumental evaluation of the axial involvment t, with x-ray of the spine and pelvis every 5 years, and MRI of the spine and pelvis every 2 years.

Diagnostic assessment: peripheral involvement, with joint ultrasound at baseline, at 3 months from the start of a new therapy, and therefore in the event of reactivation of the disease

Study summary

Spondyloarthritis (SpA) is a group of chronic inflammatory pathologies whose progression over time is poorly defined, and in particular the clinical and instrumental elements that can predispose to a condition of disease severity are not completely known. It would be important to have an idea of what the predisposing factors are, possibly already at baseline, and possibly also at follow up, of severe disease, so as to be able to act early with more aggressive and targeted therapies on these patients, so as to achieve remission.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age \>18 years; * Diagnosis of SpA confirmed by the rheumatologist with duration of symptoms \< * 2 years; * Signature of the written informed consent to the study Exclusion Criteria: * Age \< 18 years; * Patients suffering from other rheumatic pathologies (even in overlap), or genetic diseases such as Marfan syndrome, Ehlers Danlos syndrome * Any medical or psychiatric condition that in the judgment of the investigator would prevent the participant from complying with the protocol or completing the study according to the protocol. * Refusal to sign the informed consent to the study.

Primary outcome measure(s)

  • spondyloarthritis severity — t0 baseline 3hours, t1 3 months 3hours,t2 6 months 3hours,t2 12months 3hours,every six months up to the tenth year
    evaluation of disease severity at 10 years in the entire study population

Trial sites (1)

FacilityCityRegionStatus
Fondazione Policlinico Universitario A. Gemelli IRCCS Roma Italy
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06261931 on ClinicalTrials.gov ↗ ← All trials in Italy