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NCT01508975 Clinical Trial

Satiety Response of White and Brown Rice Compared to Glucose Control

Food Selection Clinical Trial

Official title:
Satiety Response of White and Brown Rice Compared to Glucose Control

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01508975
Other study ID # 11028E03765
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2011
Est. completion date December 2012

Study information
Verified date October 2019
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that consumption of either white or brown rice will be more satiating than glucose control.

Description:

This study is an acute, randomized, repeated measures design with 20 subjects. Subjects will consume 3 test breakfasts, white rice, brown rice, or glucose control, each containing 400 calories. Treatments will be one week apart. After consumption of the controlled breakfast, subjects will complete visual analogue scales (VAS) for satiety response. Additionally, they will consume a pizza lunch and record food intake for the next 24 hours. Breath gas samples will be collected to estimate fermentation of fiber in the large intestine. Also, subjective data on gastrointestinal tolerance will be collected.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- healthy subjects

Exclusion Criteria:

- inability to consume rice for breakfast

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• White Rice, Brown Rice, Glucose
white rice, brown rice, glucose

Locations
Country Name City State
United States Department of Food Science and Nutrition Saint Paul Minnesota

Sponsors (1)
Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Satiety Visual analogue scales (subjective measurements) 4 hours following breakfast
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