- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02732353
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
Status
Unknown
Conditions
Intervention / Treatment
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
- Name: Kasper Dideriksen, PhD
- Phone Number: +45 35313948
- Email: kasperjuel@hotmail.com
Study Contact Backup
- Name: Lars Holm, PhD
- Email: larsh@sund.ku.dk
Study Locations
-
-
-
Copenhagen NV, Denmark, 2400
- Bispebjerg Hospital
-
Principal Investigator:
- Kasper Dideriksen, PhD
-
Contact:
- Kasper Dideriksen, PhD
- Phone Number: +45 35313948
- Email: kasperjuel@hotmail.com
-
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.
Sponsor
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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