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UCAN CAN-DU: Canada-Netherlands Personalized Medicine Network in Childhood Arthritis and Rheumatic Disease

UCAN CAN-DU: Canada-Netherlands Personalized Medicine Network in Childhood Arthritis and Rheumatic Disease - UCAN CAN-DU

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55655
Enrollment
1400
Registered
2019-03-06
Start date
2019-03-28
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

JIA juvenile idiopathic arthritis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
No minimum to 64 Years

Inclusion criteria

Inclusion criteria: For cohorts 1,2 and 3: •

Exclusion criteria

Exclusion criteria: Cohort 1 - Biologic Basis of JIA: * Arthritis explained by any other cause * Joint injections as previous treatment Cohort 2 - Start Biologics: * Arthritis explained by any other cause * Start on biologics as an indication for uveitis only Cohort 3 - : Stop Biologics * Tapering scheme > 12 months to complete biologics stop * Continuing conventional DMARDs beyond the stop of biologics Cohort 4 - Extreme phenotypes *Arthritis explained by another diagnosis

Design outcomes

Primary

MeasureTime frame
This is a non-interventional, observational cohort study, in which we aim to standardize the assessment of disease activity in all JIA patients at baseline visit, T = 6 months and T= 12 months after start of disease, start of biological therapy and stop of biological therapy.

Secondary

MeasureTime frame
- To develop a disease classification system that categorizes children with arthritis based on their biology and clinical data. - To develop a predictive tool for treatment response to 1st (or subsequent) biological - To develop a predictive tool for successful stop of biological therapy. - To determine disease activity at T= 2 and T =5 years after diagnosis - To determine treatment response at T=2 and 5 year after start of biological therapy - To register severe adverse events in our cohort in the next 5 years. - To assess the current socioeconomic impact of this chronic disease in families with an affected child with JIA.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)