Clinical Trials Directory

Trials / Completed

CompletedNCT01925287

Oral Bioavailability of Curcumin From Micronized Powder and Liquid Micelles in Healthy Young Women and Men

Novel Strategies for the Enhancement of the Potency of Nutraceuticals With Low Oral Bioavailability and Their Application in Novel Functional Foods for Optimum Protection of the Aging Brain

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
23 (actual)
Sponsor
University of Hohenheim · Academic / Other
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

Background: The oral bioavailability of curcumin is low due to its limited intestinal uptake, rapid metabolism and excretion from the body. Considering its potent reported health-beneficial properties, researchers have tried to increase its bioavailability as a means to enhance its biological activities. Objective: The aim of the project was to develop novel curcumin formulations with enhanced oral bioavailability and to study the safety of the formulations and potential sex-differences in humans. Design: In this single-blind crossover study with three arms separated by ≥1-week washout periods, healthy subjects (13 women, 10 men) were provided standardized meals and took, in random order, a single oral dose of 500 mg curcumin as native powder, micronized powder, or liquid micelles. Blood and urine samples were collected in intervals for 24 h and total curcumin, demethoxycurcumin, and bis-demethoxycurcumin were quantified.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTcurcumin500 mg curcumin were given orally either as native powder, micronized powder, or liquid micelles

Timeline

Start date
2011-10-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2013-08-19
Last updated
2016-10-25

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01925287. Inclusion in this directory is not an endorsement.