- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00980941
Types of Starch and Their Effect on Blood Glucose, Appetite and Food Intake
September 18, 2009 updated by: University of Toronto
The Effect of Different Types of Starch on Glycemic Response, Subjective Appetite and Short-term Food Intake in Young Men
The investigators hypothesize that different types of starch vary in their effects on appetite, blood sugar and food intake.
In this study, subjects consumed five soups containing 50 g of whole grain, high amylose corn, regular corn or maltodextrin starches or no added starch at one week intervals.
The investigators measured food intake at 30 minutes, appetite and blood sugar.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
17
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Toronto, Ontario, Canada, M5S 3E2
- Department of Nutritional Studies, University of Toronto
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 30 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Healthy males with a BMI of 20-24.9 kg/m2
Exclusion Criteria:
- Females
- Smokers
- Breakfast skippers
- Individuals with diabetes or other metabolic diseases
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Soup with no added starch
|
|
|
Experimental: Soup + 50 g of whole grain starch
|
|
|
Experimental: Soup + 50 g of high amylose corn starch
|
|
|
Experimental: Soup + 50 g of regular corn starch
|
|
|
Experimental: Soup + 50 g maltodextrin starch
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Blood glucose
Time Frame: 0-170 min
|
0-170 min
|
|
Food intake
Time Frame: at 30 min after the treatment
|
at 30 min after the treatment
|
|
Appetite
Time Frame: 0-170 min
|
0-170 min
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Water intake
Time Frame: at 30 min
|
at 30 min
|
|
Palatability of treatments
Time Frame: 0-170 min
|
0-170 min
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Harvey Anderson, Ph.D., University of Toronto
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2007
Primary Completion (Actual)
April 1, 2008
Study Completion (Actual)
June 1, 2009
Study Registration Dates
First Submitted
September 18, 2009
First Submitted That Met QC Criteria
September 18, 2009
First Posted (Estimate)
September 21, 2009
Study Record Updates
Last Update Posted (Estimate)
September 21, 2009
Last Update Submitted That Met QC Criteria
September 18, 2009
Last Verified
September 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- Starch study 1
- National Starch_ethics_21513
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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