Clinical Trials Directory

Trials / Completed

CompletedNCT04256746

Dose Response Study of a Natural Extract for Reducing Post Prandial Blood Glucose

A Natural Extract for Reducing the Post Prandial Blood Glucose Response in Healthy Indian Adults: A Dose-response Study of Efficacy and Tolerance

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
84 (actual)
Sponsor
Unilever R&D · Industry
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

Randomized, balanced incomplete block design dose response study of efficacy, with 4 different dosages of mulberry fruit powdered extract added to cooked rice compared to a reference treatment (cooked rice only).

Detailed description

Dose response study with 4 dosages of mulberry fruit powdered extract (0.37, 0.75, 1.12 and 1.5 g) added to cooked rice, compared to cooked rice only(reference) on post prandial blood glucose response in healthy Indian adults. In addition, 1.5 g of mulberry fruit powdered extract was added to instant rice porridge and compared to instant rice porridge only as positive control (replication of previous research. In total there were 7 test products in the study: 5 active treatments and 2 reference treatments. The study was a cross-over study (4 interventions per subject, 4 out of the 7 test products). The recovery period between treatments was at least seven days.

Conditions

Interventions

TypeNameDescription
OTHERBoiled Rice
OTHERBoiled Rice+0.37 gr mulberry fruit powdered extract
OTHERBoiled Rice+0.75 gr mulberry fruit powdered extract
OTHERBoiled Rice+1.12 gr mulberry fruit powdered extract
OTHERBoiled Rice+1.50 gr mulberry fruit powdered extract
OTHERRice Porridge
OTHERRice porridge+1.50 gr mulberry fruit powdered extract

Timeline

Start date
2012-09-24
Primary completion
2012-10-19
Completion
2012-10-19
First posted
2020-02-05
Last updated
2020-02-05

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT04256746. Inclusion in this directory is not an endorsement.