Clinical outcomes of Japanese rheumatoid arthritis patients in real world commencing targeted therapy (CORRECT)
Not Applicable
Recruiting
- Conditions
- Rheumatoid arthritis
- Registration Number
- JPRN-UMIN000007115
- Lead Sponsor
- Tokyo Medical and Dental University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 2000
Inclusion Criteria
Not provided
Exclusion Criteria
A patient who has any of the following will be excluded from our study. 1. When a patient withdraw consent to this study 2. When a patient is participating in a clinical trial for approval of drugs at the enrollment. 3. When a patient is regarded as inappropriate to join the study based on medical reasons or other rational reasons by attending physicians' discretion.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Safety outcomes : Incidence rate and type of serious adverse events 2.Efficacy outcomes : Clinical response over time by EULAR response criteria
- Secondary Outcome Measures
Name Time Method 1.Safety outcomes : Mortality, Risk factor for serious adverse event 2.Efficacy outcomes : Achievement rates of remission or low disease activity status, achievement of functional remission, drug retention rates.