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The effect of Janus Kinase inhibitors on the heart in Rheumatoid Arthrtis

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-520710-58-00
Acronym
NL77572.029.21
Enrollment
105
Registered
2025-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-09

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

Conditions

Diagnosis of RA according to the ACR/EULAR 2010 criteria without a history of cardiovascular diseases, Rheumatroid Arthritis

Brief summary

The main study parameter is the change in LV function in RA patients after 1 year of treatment with filgotinib. LV function will be assessed at baseline and follow-up using CMR measurements of global circumferential, longitudinal and radial strain

Detailed description

The comparisons between baseline and follow-up data in RA patients treated with filgotinib for 1 year. And comparisons between RA patients and age- and sex-matched healthy volunteers. The first category is subdivided into endpoints derived from CMR, endpoints derived from CCTA, and endpoints concerning clinical treatment evaluation. The second category is subdivided into endpoints derived from CMR and endpoints derived from CCTA.

Interventions

Sponsors

Reade revalidatie & reumatologie centrum te Amsterdam
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The main study parameter is the change in LV function in RA patients after 1 year of treatment with filgotinib. LV function will be assessed at baseline and follow-up using CMR measurements of global circumferential, longitudinal and radial strain

Secondary

MeasureTime frame
The comparisons between baseline and follow-up data in RA patients treated with filgotinib for 1 year. And comparisons between RA patients and age- and sex-matched healthy volunteers. The first category is subdivided into endpoints derived from CMR, endpoints derived from CCTA, and endpoints concerning clinical treatment evaluation. The second category is subdivided into endpoints derived from CMR and endpoints derived from CCTA.

Countries

Netherlands

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026