Clinical trial on the efficacy and safety for the dysuria of the mixture of Peucedanum japonicum, nobiletin and tomato lycopene
Not Applicable
- Conditions
- rine storage disorder (urinary frequency, nocturia, urgency, urge incontinence)
- Registration Number
- JPRN-UMIN000048622
- Lead Sponsor
- Southen Knights' Laboratory Co. Ltd.
- Brief Summary
Shinryo to Shinyaku, 2020; 57: 501-511
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1 micturition disorder in treatment 2 Within 2 months from the end of treatment for micturition disorder 3 have no sense of urination 4 dysuria is the main symptom 5 Communication of the will is difficult 6 Allergies to ingredients and drugs 7 Others that the doctor in charge judged that registration to this study was inappropriate
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method