The clinical research evaluating intradermal administration with the intradermal injection system
Not Applicable
- Conditions
- healthy individuals patients taking steroid
- Registration Number
- JPRN-UMIN000010777
- Lead Sponsor
- Department of Dermatology, Kyoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
-A person who has any abnormality in the application site. -A person who are deemed to have experience or high risk of hypersensitivity for drugs used in this study. -A person who are deemed to have high risk to ultra-sound imaging examination. -Those who have experience gave rise to skin conditions such as contact dermatitis due to materials of the products (such as stainless steel and silicone oil) used in this study. -Those who are deemed inappropriate to participate in this study by doctor.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Skin property Injection site examination Injection Pain Skin image examination
- Secondary Outcome Measures
Name Time Method