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Clinical Trials/NCT00794404
NCT00794404
Completed
Not Applicable

Evaluation of Power Doppler US Technique for the Diagnosis of Spondylarthropathy in Patients With Uncertain Diagnosis Consulting for Clinical Symptoms Suggestive of Spondylarthropathy

Dr Maria-Atonietta D'AGOSTINO6 sites in 1 country489 target enrollmentDecember 2004

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spondylarthropathy
Sponsor
Dr Maria-Atonietta D'AGOSTINO
Enrollment
489
Locations
6
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to evaluate the interest of enthesis sonography for the diagnosis of spondylarthritis, in patients with uncertain diagnosis consulting for clinical symptoms suggestive of spondylarthritis

Detailed Description

Spondylarthritis (SPA) are the second most frequent inflammatory rheumatic disorders and, because it starts early in life and has a chronic progressive course, the impact of this disease on health resources and patient's life quality can be important. Because the characteritic signs of SPA, like radiological evidence of sacro-iliitis, appear late in time, the lag time between the onset first signs of SPA for the patient and the confirmed diagnosis can be very long (up to 8 years). Previous studies proved that patients who are affected by SPA are showing abnormal vascularization of peripheral enthesis more frequently than patients affected by other rheumatic diseases. Ultrasonography in B mode combined with power Doppler (PDUS) is a non invasive and highly sensitive toll which can detect enthesitis and abnormal vsacularization even for the patients who are not showing yet the evidence of SPA's symptomatology. Using PDUS as a early diagnosis tool could lead to the improvement of diagnostic procedures and therapeutic management of SpA and reduce the cost of diagnosis for patient and health insurances.

Registry
clinicaltrials.gov
Start Date
December 2004
End Date
December 2010
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Dr Maria-Atonietta D'AGOSTINO
Responsible Party
Sponsor Investigator
Principal Investigator

Dr Maria-Atonietta D'AGOSTINO

PU-PH

Groupe Français d'Etude Génétique des Spondylarthropathies

Eligibility Criteria

Inclusion Criteria

  • patients \< 50 years old, consulting for spinal inflammatory symptoms \> 3 months duration
  • patients consulting for arthritis or tenderness joints \> 3 months duration
  • patients \< 50 years old consulting for enthesitis or dactylitis \> 3 months duration
  • patients with uveitis and HLA-B27 positivity
  • relatives of SpA patients consulting for symptoms suggestive of SpA

Exclusion Criteria

  • patient with confirmed diagnosis of rheumatic disease (included SpA)
  • patient protected by law (patient \<18 years old, pregnant woman)
  • patient who can't atempt the RMI
  • patient who will have difficulties to complete the two years of follow-up

Outcomes

Primary Outcomes

Not specified

Study Sites (6)

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