Research for long term prognosis of severe cutaneous adverse reactio
Not Applicable
- Conditions
- severe cutaneous adverse reaction
- Registration Number
- JPRN-UMIN000009452
- Lead Sponsor
- Department of Dermatology, Kyorin University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
The severe cutaneous adverse reaction patients who administered in our hospital, but still visiting our department will be excluded.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ong term prognosis of severe cutaneous adverse reaction will be assessed.
- Secondary Outcome Measures
Name Time Method