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Nutrient Synergy in Beef and Stimulation of Protein Synthesis in Elderly

Nutrient Synergy in Beef and Stimulation of Protein Synthesis in Elderly

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01415973
Enrollment
20
Registered
2011-08-12
Start date
2011-07-31
Completion date
2012-01-31
Last updated
2012-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

beef, protein, synergy, intact beef constituents, protein constituent, Nutrient Synergy

Brief summary

This study will compare the effects of cooked, ground beef to those of beef protein isolate on blood and muscle proteins.

Detailed description

STUDY OBJECTIVES Primary: To compare the effects of consumption of a 3-ounce serving of beef to that of a 20g serving of BPI on skeletal muscle synthetic and breakdown rate in healthy elderly subjects. Secondary: To investigate the effect the study products on plasma levels of amino acids, insulin, and glucose in healthy elderly subjects.

Interventions

DIETARY_SUPPLEMENT3 ounces of cooked, 85% lean ground beef

Consumed once per subject.

DIETARY_SUPPLEMENT20 grams beef protein isolate

Subjects would drink 200 ml water mixed with 20 grams of beef protein isolate one time.

Sponsors

University of Arkansas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Healthy male or female. * Age 60 years or older.

Exclusion criteria

* Any (history of) gastrointestinal disease that interferes with GI function * Diagnosed and active treatment of Diabetes Mellitus type I or II * History of congestive heart failure * Recent (6 months) hospitalization for heart disease treatment or management (e.g. PTCA, stent, surgery) * Myocardial infarction in the past year * Infection or fever in the 7 days prior to enrollment * Current use of corticosteroids, growth hormone, or testosterone * Adherence to a weight loss diet * Use of protein-containing or amino acid-containing nutritional supplements within one week of enrollment * Current alcohol (\>7 ETOH per week) or drug abuse * Platelet count (PLT) \< 100,000 * History of hypo- or hyper-coagulation disorders including use of a coumadin derivative * Currently taking anti-thrombotics and cannot stop for 7 days (i.e. medical indication) * Allergy to local anesthetic * Blood hemoglobin \< 9.0 g/dL * Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements

Design outcomes

Primary

MeasureTime frameDescription
skeletal muscle synthetic and breakdown rateday oneUsing stable isotope infusion/ingestion methodology, we will measure plasma and skeletal muscle metabolic rate. Our primary end points will be muscle protein fractional synthesis rate (FSR) and whole body protein turnover rate.

Secondary

MeasureTime frameDescription
concentrations of plasma amino acids, insulin and glucoseday oneSecondary endpoints are concentrations of plasma amino acids, insulin and glucose.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026