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An observational study For Investigating success in achieving clinical, structual and functional Remission and Sustaining efficacy with Tocilizumab

Not Applicable
Conditions
Rheumatoid Arthritis
Registration Number
JPRN-UMIN000007086
Lead Sponsor
niversity of Occupational and Environmental Health, Japan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
710
Inclusion Criteria

Not provided

Exclusion Criteria

No criteria

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Percentages of three different remissions; clinical remission (the disease activity score using the 28 joint count [DAS28]-ESR), structural remission (modified total Sharp score [mTSS]), and functional remission (health assessment questionnaire [HAQ] at week 104 after tocilizumab treatment.
Secondary Outcome Measures
NameTimeMethod
Maintenance period of clinical , structual and functional remission
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