The effects of Keishi-bukuryo-gan-ryo-ka-yokuinin on fatigue --- A placebo-controlled, double-blind study
Phase 4
- Conditions
- Easy fatigability
- Registration Number
- JPRN-UMIN000001532
- Lead Sponsor
- Polyene Project, Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
Those who have histories of or are suffering from serious diseases or metabolic/endocrine diseases. Those who are allergic to KBKY. Those of frail constitution. Menopausal women. Those who are pregnant, lactating or planning to be pregnant. Those who are not suitable for the study according to the doctors in charge of this trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method