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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01673321
Other study ID # 27226
Secondary ID
Status Completed
Phase N/A
First received August 22, 2012
Last updated August 24, 2012
Start date February 2012
Est. completion date June 2012

Study information

Verified date August 2012
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

This study compared the effects of dairy products, including milk and yogurt, with different amounts of proteins on responses of appetite, glucose and insulin and on food intake at a meal served 120 minutes later in healthy adult male individuals.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 2012
Est. primary completion date June 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria:

- Age: 20-30 years

- Body mass index: 20 and 24.9 kg/m2

Exclusion Criteria:

- Breakfast skippers,

- Smokers,

- Dieters,

- Individuals with lactose-intolerance or who are allergic to milk,

- Individuals with gastrointestinal problems and

- Individuals with diabetes or other metabolic diseases

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Dietary intervention
All snacks (arms) were randomly given to subjects to be consumed within 5 minutes, after 4 hours of consuming a standard breakfast.

Locations

Country Name City State
Canada Department of Nutritional Sciences, University of Toronto Toronto Ontario

Sponsors (4)

Lead Sponsor Collaborator
University of Toronto Dairy Farmers of Ontario, Mondelez International, Inc., Natural Sciences and Engineering Research Council, Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Appetite Appetite scores in the pre- and post-test meal periods Pre-(0-120 min) and post-(120-260 min) meal periods No
Primary Food intake Calories consumed at the test meal 120 minutes after consumption of treatments No
Secondary Glycemia Glycemic responses in the pre- and post-test meal periods Pre-(0-120 min) and post-(120-260 min) meal periods No
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