A study for the difference in effects of high-dose prednisolone therapy for autoimmune disease patients
Not Applicable
Recruiting
- Conditions
- rheumatic disease like dermatomyositis, polymyositis, systemic lupus erythematosus, vasculitides, adult Still's disease and so on.
- Registration Number
- JPRN-UMIN000007673
- Lead Sponsor
- Graduate School of Medicine Kyoto University Rheumatology and Clinical Immunology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who have taken oral prednisolone for long time Patients who have allergy to prednisolone
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of the Disease activity of rheumatic diseases 2 weeks after the induction of oral prednisolone therapy
- Secondary Outcome Measures
Name Time Method