Comparison of bioavailability of curcuminoid-containing turmeric supplements after single oral administration in humans: a double-blind, four-way crossover study
Not Applicable
- Conditions
- Healthy subjects
- Registration Number
- JPRN-UMIN000016493
- Lead Sponsor
- Health Evaluation Research Office Kobe University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 9
Inclusion Criteria
Not provided
Exclusion Criteria
Severe disease history Food or drug allergy Regular use or use within 2 weeks of turmeric-containing drugs or supplements
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plasma concentrations of curcuminoids and related pharmacokinetics parameters
- Secondary Outcome Measures
Name Time Method Safety (biochemical examination of blood, medical examination by interview)