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The comparison of effectiveness between intravenous and subcutaneous administration route of tocilizumab in patients with rheumatoid arthritis

The comparison of effectiveness between intravenous and subcutaneous administration route of tocilizumab in patients with rheumatoid arthritis - The comparison of effectiveness between intravenous and subcutaneous administration route of tocilizumab in patients with rheumatoid arthritis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000028261
Enrollment
100
Registered
2017-07-17
Start date
2017-02-01
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 arthritis

Interventions

None listed

Sponsors

Osaka City University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: RA patients fulling the American Rheumatology Association criteria 1987 and ACR/EULAR classification cliteria 2010. The patients started tocilizumab therapy.

Exclusion criteria

Exclusion criteria: Patients with other diseases that can affect the infllamation state. Patients who was deemed inappropriate by test doctor to participate in this study.

Design outcomes

Primary

MeasureTime frame
The comparison of ultrasonographic findings between intravenus and subcutaneous administration route of tocilizumab

Countries

Japan

Contacts

Public ContactTadashi Okano

Osaka City University Medical School Orthopedic Surgery

ma1sa3ru@med.osaka-cu.ac.jp0666453851

Outcome results

None listed

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