rheumatoid Arthritis
Conditions
Interventions
None listed
Sponsors
Osaka City University Medical School, Center for Senile Degerative Disorders (CSDD)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who were resistant for DMARDs (including MTX) or anti-TNF biologics therapy, and then will receive tocilizumab therapy
Exclusion criteria
Exclusion criteria: Patients who received tocilizumab therapy previously Patients who received steroid newly, dose-up of steroid, plasma exchange or artificial joint replacements within 4 weeks before tocilizumab treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| DAS28 and CDAI at 12 week after the start of tocilizumab therapy | — |
Secondary
| Measure | Time frame |
|---|---|
| DAS28 and CDAI at 28 week after the start of tocilizumab therapy Adverse event | — |
Countries
Japan
Contacts
Public Contacttatsuya Koike
Osaka City University Medical School Center for Senile Degerative Disorders (CSDD)
Outcome results
None listed