investigator initiated study of Rhododenol-induced Leukoderma
Not Applicable
- Conditions
- Rhododenol-induced Leukoderma
- Registration Number
- JPRN-UMIN000023244
- Lead Sponsor
- Teikyo University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 10
Inclusion Criteria
Not provided
Exclusion Criteria
1)Age under twenty years old at the time of informed consent. 2)Those who were suspected of concomitant vitiligo vulgaris. 3)Those who show skin problems such as erythema at the site of target region. 4)Those who show allagic reaction against Bimatoprost. 5)Those women who are pregnant or possibly pregnant or during lactation or those who cannot agree with contraception during the study. 6)Those otherwise principal physician considered unsuitable to include in this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method