A study of the concentration of povidone-iodine that causes false positive in intradermal test
Not Applicable
- Conditions
- not applicable
- Registration Number
- JPRN-UMIN000050625
- Lead Sponsor
- agoya University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 4
Inclusion Criteria
Not provided
Exclusion Criteria
Those who are allergic to ingredients of povidone-iodine Those who are allergic to alcohol Those who are taking drugs that may affect intradermal tests, such as steroids and antihistamines Those who have a history of allergies due to food, medicines, or cosmetics Those with skin disease currently being treated Under the age of 18
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the diameter of initial wheal just after injection and 20 min post-injection at each concentration of povidone-iodine
- Secondary Outcome Measures
Name Time Method