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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01812967
Other study ID # Milk Components Study
Secondary ID
Status Completed
Phase N/A
First received March 13, 2013
Last updated March 15, 2013

Study information

Verified date March 2013
Source University of Toronto
Contact n/a
Is FDA regulated No
Health authority Canada: University of Toronto Research Ethics Board
Study type Interventional

Clinical Trial Summary

The investigators hypothesize that the physiological effects of milk on satiety and glycemic control are mediated by the interaction between its macronutrient components by both insulin-dependent and independent mechanisms.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date September 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 30 Years
Eligibility Inclusion Criteria:

- Healthy young men

- 20-30 years of age

- BMI: 20-24.9 kg/m2

Exclusion Criteria:

- Smoking

- Dieting

- Skipping breakfast

- Lactose intolerance or allergies to milk

- Taking medications that may affect glucose metabolism or appetite

- Diabetes (fasting blood glucose = 7.0 mmol/L) or other metabolic diseases

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Milk Fat

Milk Protein

Lactose

Other:
Whole milk (3.25% M.F.(
Commercially available milk from the grocery store
Dietary Supplement:
Simulated Milk Beverage
Added lactose + fat + protein together to form a mixture

Locations

Country Name City State
Canada University of Toronto Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
University of Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Gastrointestinal hormones and gastric emptying rate Gatrointestinal hormones measured include plasma concentrations of glucagon-like peptide-1 (GLP-1), peptide tyrosine tyrosine (PYY), cholecystokinin (CCK), and ghrelin.
Gastric emptying is assessed indirectly by adding 1.5 g of paracetamol (acetaminophen) to each beverage and measuring plasma paracetamol concentrations.
0-180 min No
Primary Glucose 0-180 min No
Secondary Insulin 0-180 min No
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