Determination of the PPG and Insulin Responses of Rice Alone and Rice Consumed With Sugardown™

Determination of the Postprandial Glucose And Insulin Responses of White Rice Alone And White Rice Consumed With Sugardown™

This study was a partly controlled laboratory-based study comparing the short-term postprandial blood glucose and insulin responses produced by 3 test meals containing white rice alone or with SUGARDOWN™ (Galactomannan) in overweight adults.

Study Overview

• Status: Completed
• Conditions: Postprandial Hyperglycemia
• Intervention / Treatment: Dietary supplement: Sugardown™; Dietary supplement: Rice

Detailed Description

STUDY SUMMARY This study was a partly controlled laboratory-based study comparing the short-term postprandial blood glucose and insulin responses produced by three test meals containing white rice alone or with SUGARDOWN™ (Galactomannan) in overweight adults. In the study, subjects were their own controls. Effects of the two test meals containing SUGARDOWN™ were compared to the effects produced by test meals containing an equal-carbohydrate portion of white rice alone (the control meal). The study used a repeated-measures design, such that every subject consumed each meal on two separate occasions, completing a total of six separate test sessions. Each subject completed their test sessions on separate weekday mornings at a similar time of day, as close as possible to the time they would normally eat breakfast.

SUBJECTS Ten healthy, non-smoking, overweight or obese subjects (4 females, 6 males) voluntarily participated in this study. The mean ± SD age of the subjects was 29.2 ± 3.3 yr (range: 25.6 - 36.8 yr), and their mean ± SD body mass index value was 27.3 ± 1.1 kg/m2 (range: 25.5 - 28.7 kg/m2).

Volunteers were given detailed written and verbal information about all of the study's inclusion criteria and experimental procedures. If the volunteers decided that they would like to participate in the study, they were asked to come to the research centre on another morning, where they completed a detailed screening questionnaire that assessed their current health status and medical history. In order to participate in the study, the volunteers had to meet the inclusion criteria listed below. All suitable volunteers that were invited to participate in the study were required to sign a detailed subject information sheet and a consent form before commencing any experimental procedures.

• Study Type: Interventional
• Enrollment (Actual): 10
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 25 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Aged between 25-65 years.
• Non-smoker.
• Stable body weight within the overweight weight range for their height (BMI values > 25 kg/m2).
• Normal dietary habits; not dieting or eating in an overly restrictive fashion in the past 3 months.
• A regular pattern of low to moderate physical activity.
• Able to fast for ≥ 10 hours the night before each test session.
• Able to refrain from eating a legume-based evening meal or drinking alcohol the day before each test session.
• Finds the test foods suitable for consumption within 12 minutes.
• Participant covered by social security or a similar system.
• Not taking any treatment for anorexia, weight loss, or any form of treatment or medication likely to interfere with metabolism or dietary habits.
• Signed the informed consent form for the study.

Exclusion Criteria:

• Currently following a restrictive diet (low-calorie, low-carbohydrate, vegan).
• Any clinically significant physical or mental illness.
• Suffering from a food allergy or serious food intolerance.
• Regularly taking prescription medication other than standard contraceptive medication.
• Females who are currently pregnant, breast-feeding, trying to become pregnant or not using an acceptable contraceptive.
• Participating in another clinical trial or participated in another clinical trial within the last week.
• Undergoing general anaesthesia in the month prior to inclusion.
• Subject in a situation, which in the investigator's opinion could interfere with optimal participation in the present study or could constitute a special risk for the subject.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: None (Open Label)

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 3 tablets Sugardown™; Repeated-measures, open cross-over design: 10 subjects consumed three different test meals comprising of white rice consumed with 3 tablets Sugardown™	Dietary supplement: Sugardown™; Test food #2: White Rice < 63.0 g (dry) Jasmine rice + 3 Sugardown™ tablets consumed together with 250 mL water Test food #3: White Rice < 63.0 g (dry) Jasmine rice + 6 Sugardown™ tablets consumed together with 250 mL water; Other Names: PAZ320; BTI320
Placebo Comparator: Rice only; Repeated-measures, open cross-over design: 10 subjects consumed three different test meals comprising of white rice	Dietary supplement: Rice; Test food #1: White Rice <63.0 g (dry) Jasmine rice consumed together with 250 mL water; Other Names: PAZ320; BTI320
Experimental: 6 tablets Sugardown™; Repeated-measures, open cross-over design: 10 subjects consumed three different test meals comprising of white rice consumed with 6 tablets Sugardown™	Dietary supplement: Sugardown™; Test food #2: White Rice < 63.0 g (dry) Jasmine rice + 3 Sugardown™ tablets consumed together with 250 mL water Test food #3: White Rice < 63.0 g (dry) Jasmine rice + 6 Sugardown™ tablets consumed together with 250 mL water; Other Names: PAZ320; BTI320

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Postprandial increment glucose under the area curve (iAUC)	Blood samples were collected into a micro-centrifuge tube containing the anticoagulant, heparin sodium salt. Plasma glucose concentrations were measured in duplicate using a spectrophotometric centrifugal analyser employing the glucose hexokinase/glucose-6-phosphate dehydrogenase enzymatic assay.	2 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Postprandial increment insulin under the area curve (iAUC)	Each blood sample was collected into a micro-centrifuge tube containing the anticoagulant. Plasma insulin concentrations were measured using a solid phase antibody-coated tube radioimmunoassay kit.	2 days

Collaborators and Investigators

• Sponsor: Boston Therapeutics
• Investigators: Principal Investigator: Jennie Brand-Miller, Prof., Human Nutrition Unit School of Molecular Bioscience, University of Sydney, Australia

Study record dates

Study Major Dates

• Study Start (Actual): March 1, 2011
• Primary Completion (Actual): June 1, 2011
• Study Completion (Actual): June 1, 2011

Study Registration Dates

• First Submitted: February 11, 2014
• First Submitted That Met QC Criteria: December 12, 2017
• First Posted (Actual): December 18, 2017

Study Record Updates

• Last Update Posted (Actual): December 18, 2017
• Last Update Submitted That Met QC Criteria: December 12, 2017
• Last Verified: December 1, 2017

More Information

Terms related to this study

• Keywords: Insulin; Postprandial blood glucose; Galactomannan; SUGARDOWN™
• Additional Relevant MeSH Terms: Glucose Metabolism Disorders; Metabolic Diseases; Hyperglycemia; Hypoglycemic Agents; Physiological Effects of Drugs; PAZ320
• Other Study ID Numbers: PAZ320-001