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Medical Follow-up of New Cases of Polyarthritis in Children and Young Adults

Recruiting
Conditions
Juvenile Idiopathic Arthritis
Rheumatoid Arthritis
Diffuse Systemic Sclerosis
Seronegative Arthritis
Psoriatic Arthritis
Systemic Lupus Erythematosus
Registration Number
NCT07000916
Lead Sponsor
Université Catholique de Louvain
Brief Summary

Population:

Juvenile idiopathic arthritis (JIA), rheumatoid arthritis (RA) and seronegative / psoriatic / undifferentiated arthritis (UA), systemic lupus erythematosus (SLE) or diffuse systemic sclerosis dSS).

Naïve to basic treatment OR treated for ≤ 3 months; except for patients with JIA.

These 5 cohorts will be subject to standardized clinical monitoring.

Detailed Description

This study is proposed by the Rheumatology and Pediatrics departments of the 3 French-speaking Universities.

The first objective will be to include a progressive number of new young patients (≤ 50 years) in order to optimize and standardize care and clinical response objectives. The number of 25% of new incident cases will be sought with an increase of 20% each year during the 5 to 10 years of this project.

Population: JIA, RA/UA, SLE, dSS (American Congres of Rheumatology criteria). Naïve to basic treatment OR treated for ≤ 3 months; except for patients with JIA.

These 5 cohorts will be subject to standardized clinical monitoring and specific objectives that will make it possible to analyze the number of patients with a good control of the disease and/or a clinical remission, defined according to the international criteria.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
1000
Inclusion Criteria
  • Diagnosis of juvenile idiopathic arthritis, rheumatoid arthritis and seronegative / psoriatic / undifferentiated arthritis, systemic lupus erythematosus or diffuse systemic sclerosis (ACR criteria).
  • Naïve to basic treatment OR treated for ≤ 3 months; except for patients with JIA.
Exclusion Criteria
  • Treated for > 3 months
  • > 50 years old

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Remission rate or absence of synovitis in Rheumatoid arthritis patientsThrough the entire study, during approximately 15 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

UCLouvain

🇧🇪

Brussels, Belgium

UCLouvain
🇧🇪Brussels, Belgium
Patrick Durez
Contact
patrick.durez@uclouvain.be
Tatiana Sokolova
Contact
tatiana.sokolova@uclouvain.be

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