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Clinical Trials/NCT03926429
NCT03926429
Completed
N/A

A Bicentre Retrospective Study of Features and Outcomes of Patients With Reactive Arthritis

Hospices Civils de Lyon2 sites in 1 country58 target enrollmentFebruary 1, 2013
ConditionsArthritis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Arthritis
Sponsor
Hospices Civils de Lyon
Enrollment
58
Locations
2
Primary Endpoint
To determine the incidence of reactive arthritis in patients hospitalised in the rheumatology department
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The aim of this study is to assess the incidence and the clinical and therapeutic characteristics of reactive arthritis and to compare them with those of a historical cohort. We hypothesised that improved hygiene together with prevention and treatment of sexually transmitted infections may have decreased the incidence of reactive arthritis.

Registry
clinicaltrials.gov
Start Date
February 1, 2013
End Date
December 31, 2014
Last Updated
7 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • reactive arthritis diagnosed in one of the two rheumatology departments from Centre Hospitalier Lyon Sud or Besançon

Exclusion Criteria

  • presence of other known causes of arthritis, such as other defined spondyloarthritides, septic arthritis, Lyme disease, microcrystalline arthritis or rheumatoid arthritis

Outcomes

Primary Outcomes

To determine the incidence of reactive arthritis in patients hospitalised in the rheumatology department

Time Frame: December 2014

Incidence of reactive arthritis in patients hospitalised in the rheumatology department

Study Sites (2)

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