Interindividual Variation in Excretion of Curcumin
Not Applicable
Completed
- Conditions
- MetabolitesGut Microbiota
- Interventions
- Dietary Supplement: curcumin
- Registration Number
- NCT03746158
- Lead Sponsor
- University of Massachusetts, Amherst
- Brief Summary
The objective of this project is to elucidate the interindividual variations in excretion of curcumin and its metabolites.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 8
Inclusion Criteria
- 18-30 year old healthy adults
Exclusion Criteria
- Exclusion criteria included those who are <18 or >30 years old, have a BMI of <20 or >29 kg/m2, have a weight change >4.5 kg in the past 3 months, exceed exercise activities of a curcumin level over the past 3 months, have any diseases, especially intestinal disorders, had abnormal liver or kidney function tests. Those who smoke, consume more than two alcoholic drinks per day, use medication affecting gut microbiota profile (e.g., antibiotics and probiotics) in past three months will also be excluded.
- Additionally, this study excludes menopausal women, those using hormone-based contraceptives, those with abnormal menstrual cycles, and those who are pregnant, lactating or planning to become pregnant.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Curcumin curcumin subjects will be assigned to consume one capsule of curcumin (330 mg of curcumin per capsule) three times a day (one capsule with each meal).
- Primary Outcome Measures
Name Time Method Determine the concentration of curcumin and its metabolites in the human fecal samples. 3-4 weeks Utilize LC-MSMS to identify and quantify the curcumin and its metabolites in the subjects fecal samples.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Institute for Applied Life Sciences
🇺🇸Amherst, Massachusetts, United States