Clinical Investigation of Keisi-bukuryogan for the treatment of symptoms in Yusho patients.
Not Applicable
- Conditions
- Certified Yusho victim
- Registration Number
- JPRN-UMIN000017463
- Lead Sponsor
- Department of Dermatology, Graduate School of Medical Sciences, Kyushu University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1) Women who have pregnancy, are nursing, or are likely to become pregnant. 2) Patients who are taking other Kampo medicines. Patients who have 4 weeks washout period for attending the study are eligible. 3) Any other patients who are regarded as unsuitable for this study by the investigators because of such as serious complication.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS score (peripheral nerve: pain, numbness, skin; acne, blotch, respiratory; cough, sputum, malaise)
- Secondary Outcome Measures
Name Time Method 1.QOL (Quality Of Life) quantitatively evaluated by SF-36. 2.Oxidative stress marker value s and anti-oxidative stress marker values. 1.Safety during treatment period.