Acute Effects of Dairy and Meat Proteins on Bone Metabolism and Metabolic Profile

NCT ID: NCT01773304

Last Updated: 2013-03-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

17 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-12-31

Study Completion Date

2013-02-28

Brief Summary

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The purpose of this randomized, controlled, cross over single meal study is to investigate the metabolic effects of a breakfast rich in dairy proteins and to determine biomarkers for their intake. The results from this project will increase our knowledge about nutritional value of dairy proteins, which is necessary to decide whether dairy products can be recommended for prevention of weight related bone loss.

Detailed Description

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Conditions

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Obesity Bone Metabolism

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Meal rich in dairy protein

Group Type EXPERIMENTAL

Dietary meal intervention

Intervention Type OTHER

Test meals with different protein types (dairy versus meat)

Meal rich in meat protein

Group Type EXPERIMENTAL

Dietary meal intervention

Intervention Type OTHER

Test meals with different protein types (dairy versus meat)

Interventions

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Dietary meal intervention

Test meals with different protein types (dairy versus meat)

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Healthy males and females between 18 and 50 years
* BMI 25-40

Exclusion Criteria

* Physical activity more than 10 hours weekly
* Smoking
* Diagnosed osteoporosis in at least one parent
* Dietary supplements and vitamin pills (during the study and 2 months before the start)
* Vegetarians and vegans
* Lactose intolerant
* Women who are pregnant, breastfeeding or post-menstrual
* Regular intake of medication
* Chronic diseases (including osteoporosis, cancer, diabetes, cardiovascular disease and mental disorders)
* Participation in other clinical trials that could affect the test results
* Donation of blod within 3 months before intervention start
* Hypersensitivity to paraaminobenzoic acid (PABA)
* Not able to comply with the procedures established by the Protocol
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Danish Agriculture and Food Council

OTHER

Sponsor Role collaborator

University of Copenhagen

OTHER

Sponsor Role lead

Responsible Party

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AAstrup

Dr Med Sci

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Department of Human Nutrition, University of Copenhagen

Copenhagen, Frederiksberg C, Denmark

Site Status

Countries

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Denmark

Other Identifiers

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M210

Identifier Type: -

Identifier Source: org_study_id

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