BCAAs, Muscle Protein Synthesis and Glucose Uptake

NCT ID: NCT06218264

Last Updated: 2025-05-29

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

RECRUITING

Clinical Phase

NA

Total Enrollment

28 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-10

Study Completion Date

2025-12-31

Brief Summary

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The present study aims to quantify the insulin sensitivity and the skeletal muscle protein synthetic response to consuming a test drink containing all amino acids or all amino acids except for BCAAs.

Detailed Description

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Twenty-eight healthy, young volunteers will receive a stable isotope tracer infusion (7.5h) combined with repeated blood and muscle sampling, to measure muscle protein synthesis rate in the postabsorptive state following ingestion of a drink containing all amino acids (n=14) or all amino acids except for BCAAs (n=14).

Conditions

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Healthy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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FullAA

Amino acid drink containing all amino acids

Group Type ACTIVE_COMPARATOR

Ingestion of an amino acid supplement

Intervention Type DIETARY_SUPPLEMENT

Oral intake of a supplement containing amino acids

NoBCAA

Amino acid drink containing all amino acids except for BCAAs.

Group Type ACTIVE_COMPARATOR

Ingestion of an amino acid supplement

Intervention Type DIETARY_SUPPLEMENT

Oral intake of a supplement containing amino acids

Interventions

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Ingestion of an amino acid supplement

Oral intake of a supplement containing amino acids

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Aged from 18-35 years
* 18.5 \< Body mass index \< 30 kg·m2
* Recreationally active (performing non-competitive physical exercise at least one time per week for minimally 30 minutes)

Exclusion Criteria

* Smoking
* Diabetes (Type 1, Type 2, or genetic form of diabetes)
* Any diagnosed cardiovascular (heart) disease or high blood pressure (≥140 mmHg systolic and/or ≥90 mmHg diastolic)
* Chronic use of any prescribed or over the counter pharmaceuticals (excluding oral contraceptives and contraceptive devices)
* Known allergy to lidocaine
* Regular use of dietary protein and/or amino acid supplements (\>3 times per week)
* Currently involved in a structured progressive resistance training programme (\>3 times per week)
* A personal or family history of thrombosis (clots), epilepsy, seizures, or schizophrenia.
* Any previous motor disorders or disorders in muscle and/or lipid metabolism
* Presence of an ulcer in the stomach or gut and/or strong history of indigestion
* Known severe kidney problems
* Pregnant or breastfeeding
* Unable to give consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Wageningen University

OTHER

Sponsor Role lead

Responsible Party

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Marlou Dirks

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Wageningen University and Research

Wageningen, Gelderland, Netherlands

Site Status RECRUITING

Countries

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Netherlands

Central Contacts

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Marlou Dirks, PhD

Role: CONTACT

+31 317 480 100

Facility Contacts

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Human and Animal Physiology

Role: primary

+31 (0) 317 484 136

Other Identifiers

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NL82984.028.23

Identifier Type: -

Identifier Source: org_study_id

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