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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00988377
Other study ID # Kraft_whey protein: study 1
Secondary ID
Status Completed
Phase N/A
First received September 30, 2009
Last updated October 1, 2009
Start date May 2007
Est. completion date November 2007

Study information

Verified date October 2009
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

The objective of this study was to describe relationships among whey protein when consumed before a meal on food intake and pre- and post-meal satiety, blood glucose in healthy young adults.


Description:

A randomized, cross-over design study was conducted. Whey protein preloads (10-40 g) were provided in 300 ml water. At 30 min following consumption, subjects were fed an ad libitum pizza meal. Satiety, and blood glucose were measured at baseline and selected intervals pre- (0, 15 and 30 min) and post-meal (50, 65, 80 and 95 min).


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date November 2007
Est. primary completion date August 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 27 Years
Eligibility Inclusion Criteria:

- healthy

- normal weight ( 18-24.9 kg/m²)

- young aged 20-27 year old

Exclusion Criteria:

- breakfast skippers

- smokers

- dieters

- individuals with diabetes (fasting BG = 7.0 mmol/L) or other metabolic diseases

Study Design

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


Related Conditions & MeSH terms


Intervention

Other:
dietary intervention
whey protein 10-40 g
water control
Iso-volumetric (300 ml) water control (Crystal Springs, Canada)

Locations

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

Sponsors (3)

Lead Sponsor Collaborator
University of Toronto 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
Primary Blood glucose subjective appetite Food intake at 30 min 0-95 min No
Secondary physical comfort palatability 0-95 min No
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