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Interindividual Variation in Excretion of Curcumin

Not Applicable
Completed
Conditions
Metabolites
Gut 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
GroupInterventionDescription
Curcumincurcuminsubjects 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
NameTimeMethod
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
NameTimeMethod

Trial Locations

Locations (1)

Institute for Applied Life Sciences

🇺🇸

Amherst, Massachusetts, United States

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