Absorption and Muscle-stimulating Effect of Hydrolyzed and Minced Beef

November 7, 2016 updated by: Kasper Dideriksen
To measure the absorption kinetics and postprandial amino acid availability after ingestion of minced beef compared with hydrolyzed beef in young males. Moreover, the basal muscle protein synthesis and the postprandial muscle protein synthetic response to minced beef and hydrolyzed beef ingestion are measured in young males. The postprandial muscle protein synthetic response is measured and compared during the early postprandial period (0-3 hours) after ingestion of the two meat products.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Copenhagen NV, Denmark, 2400
        • Bispebjerg Hospital
        • Principal Investigator:
          • Kasper Dideriksen, PhD
        • Contact:
        • Principal Investigator:
          • Søren Reitelseder, PhD
        • Principal Investigator:
          • Lars Holm, PhD

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Healthy
  • Non-obese (BMI<30)

Exclusion Criteria:

  • Chronic medical disease
  • >5 hour of exercise weekly, except light activities such as stretching/gymnastics and bike-riding/walking as transportation

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Minced beef
Cow meat protein supplement
Experimental: Hydrolyzed beef
Cow meat protein supplement

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in skeletal muscle protein fractional synthetic rate
Time Frame: During the postprandial period (0-3 hrs).
The fractional synthetic rate of skeletal muscle proteins (%/h) measured during the overnight fasted state and the postprandial state.
During the postprandial period (0-3 hrs).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Protein absorption
Time Frame: During the postprandial period (0-3 hrs).
The change in venous plasma ring-2H5-phenylalanine enrichment after ingestion of meat protein, reflects the protein absorption from the meat protein products.
During the postprandial period (0-3 hrs).
Plasma amino acid concentration
Time Frame: During the postprandial period (0-3 hrs).
Change in venous plasma amino acid concentration after ingestion of meat protein.
During the postprandial period (0-3 hrs).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Søren Reitelseder, PhD, Bispebjerg Hospital
  • Principal Investigator: Kasper Dideriksen, PhD, Bispebjerg Hospital
  • Principal Investigator: Lars Holm, PhD, Bispebjerg Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

November 1, 2016

Primary Completion (Anticipated)

March 1, 2018

Study Completion (Anticipated)

March 1, 2018

Study Registration Dates

First Submitted

March 30, 2016

First Submitted That Met QC Criteria

April 4, 2016

First Posted (Estimate)

April 8, 2016

Study Record Updates

Last Update Posted (Estimate)

November 8, 2016

Last Update Submitted That Met QC Criteria

November 7, 2016

Last Verified

November 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • H-15012327

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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