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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01255085
Other study ID # PureNet_22627
Secondary ID
Status Completed
Phase N/A
First received December 3, 2010
Last updated June 14, 2012
Start date May 2008
Est. completion date June 2011

Study information

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

Clinical Trial Summary

It is hypothesized that yellow pea protein and fiber will reduce short-term food intake, subjective appetite and glycemic response.


Description:

A within-subject, randomized study was conducted. Each subject returned 5 times, 1 week apart, and received 1 of the 5 treatments per week. The 5 treatments were tomato soup with 10 or 20 g of isolated yellow pea fibre or protein, or a control soup with no added pea fractions. Food intake was measured at an ad libitum pizza meal served 30 minutes after treatment. Satiety and blood glucose (via finger prick) were measured throughout the treatment period.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date June 2011
Est. primary completion date August 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 29 Years
Eligibility Inclusion Criteria:

- male 20-30 years old healthy weight

Exclusion Criteria:

- smoking restrictive eating metabolic diseases breakfast skippers dieters

Study Design

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


Intervention

Dietary Supplement:
yellow pea protein
Served in a tomato soup
yellow pea fiber
Served in a tomato soup
Control Tomato Soup
Served in a tomato soup

Locations

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

Sponsors (2)

Lead Sponsor Collaborator
University of Toronto Agriculture and Agri-Food Canada

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Energy Intake Energy intake at an ad libitum pizza meal at 30 minutes after treatment No
Secondary Glycemic Response Blood Glucose every 15-30 minutes via finger prick 0-170 minutes post treatment No
Secondary Subjective Appetite Subjective Appetite measured every 15-30 minutes via Visual Analog Scale (VAS) 0-170 minutes post treatment No
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