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Evaluation of cardiac risk in rheumatoid arthritis patients befoer and after treatment of Biologics in retrospective study

Evaluation of cardiac risk in rheumatoid arthritis patients befoer and after treatment of Biologics in retrospective study - Evaluation of cardiac risk in rheumatoid arthritis patients befoer and after treatment of Biologics in retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013885
Enrollment
100
Registered
2014-05-05
Start date
2012-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

rheumatoid arthiritis

Interventions

RA patients were scheduled to receive TCZ once a month after 24 weeks. Serum NT-pro BNP concentrations were measured simultaneously on stored baseline and 24 week samples.

Sponsors

Itabashi Chuo Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Consecutive RA patients with active disease without a clinical diagnosis of cardiovascular disease were enrolled. The RA patients each had inadequate clinical response to non-biologic DMARDs. RA patients were scheduled to receive Biologics after 24 weeks

Exclusion criteria

Exclusion criteria: Exclusion criteria were diabetes, previous cardiovascular events, cardiopathy, hypertension and renal disease.

Design outcomes

Primary

MeasureTime frame
Change of NT-pro BNP after treatment at 24 weeks of Biologics.

Countries

Japan

Contacts

Public ContactIsamu Yokoe

Itabashi Chuo Medical Center Rheumtology

pero1995@gmail.com03-3967-0572

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026