Quantitative Determination of Nadifloxacin in Follicles of Acne Patients Treated by Topical Nadifloxacin With or Without Adapalene and Benzoyl Peroxide
- Conditions
- Acne
- Registration Number
- JPRN-UMIN000025358
- Lead Sponsor
- Toshitatsu Nogita
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Not provided
(1) The patient who had a following treatment within 4 weeks prior to the initiation of test drug treatment Facial chemical peering, Leaser therapy, or Phototherapy (2) The patient who had a following treatment within 2 weeks prior to the initiation of test drug treatment Use of Nadifloxacin on his/her face, Facial aesthetic treatment, Use of facial cleanser with scrub (3) The patient who would use or will not stop to use agent for skin (all of prescription medicine and OTC medicine) during the period of the study (4) Pregnant woman, might be pregnant woman, and/or Breastfeeding woman (5) The patient who is hypersensitivity to ingredients of test drug (6) The patient to whom physician recognize him/her will not be included in the study because of his/her history and complication of systemic diseases (7) The patient to who is participating other clinical research or study (8) The patient to whom physician judge as inappropriate for this clinical study due to safely issues
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of Nadifloxacin in Follicles of Acne
- Secondary Outcome Measures
Name Time Method