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Muscle Anabolic Response to β2-adrenergic Stimulation With Increased Amino Acid Availability.

The Importance of Amino Acid Availability in Modulating the Muscle Anabolic Response to β2-adrenergic Stimulation.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06654986
Enrollment
36
Registered
2024-10-23
Start date
2024-10-31
Completion date
2026-12-18
Last updated
2025-04-09

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

Conditions

Healthy

Keywords

Beta2-adrenergic stimulation, Amino acid availability, Skeletal muscle hypertophy

Brief summary

The purpose of the project is to investigate the effect of amino acid availability on the muscle anabolic response to beta2-adrenergic stimulation in young healthy men and women.

Interventions

DRUGSalmeterol + amino acid availability

The participants will be administered 200 µg salmeterol (8 puffs) from a MDI device and 40 g amino acid availability (clear whey in a shaker with water) daily during a 6-week intervention. Participants will be instructed to provide documentation of both the inhalation and the shaker intake via video.

DRUGSalmeterol + placebo

The participants will be administered 200 µg salmeterol (8 puffs) from a MDI device. Furthermore they will be administered 80 g placebo (carbo fuel in a shaker with water) daily during a 6-week intervention. Participants will be instructed to provide documentation of both the inhalation and the shaker intake via video.

The participants will be administered placebo (8 puffs) from a MDI device. Furthermore they will be administered 80 g placebo (carbo fuel in a shaker with water) daily during a 6-week intervention. Participants will be instructed to provide documentation of both the inhalation and the shaker intake via video.

Sponsors

University of Copenhagen
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Thirty-six healthy, well-trained men and women will be randomized into three distinct groups, each receiving one of the following interventions: 1) salmeterol with amino acid availability, 2) salmeterol, or 3) a placebo, administered twice daily over a 6-week intervention period. This design aims to elucidate the impact of amino acid availability on the muscle anabolic response to beta2-adrenergic stimulation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 18-40 * Physically active \>5 hours a week * Maximum oxygen uptake classified as high or very high

Exclusion criteria

* Active smoker currently or within the past 5 years * Regular intake of medication deemed by the responsible study physician to affect the test parameters (hormonal contraception is accepted for women) * Chronic or acute illness deemed by the responsible study physician to affect the test parameters * Deviation from the study protocol * Lean mass index \>21 kg/m² * Pregnancy * Smoker * Blood donation during the past 3 months

Design outcomes

Primary

MeasureTime frameDescription
Skeletal muscle hypertrophyThrough study completion, an average on 7 weeksMuscle hypertrophy measured using Dual-energy X-ray Absorptiometry (DXA).

Secondary

MeasureTime frameDescription
Quadriceps strengthThrough study completion, an average on 7 weeksMaksimal torque (Nm) achieved during isometric contraction
Power output during sprint testingThrough study completion, an average on 7 weeksPower output measured in Watts during a sprint on a bike ergometer
Power output during time trialThrough study completion, an average on 7 weeksMean power output measured in Watts during a time trial on a bike ergometer

Other

MeasureTime frameDescription
Maximal oxygen uptakeThrough study completion, an average on 7 weeksMaximal oxygen uptake measured during an incremental test to exhaustion on a bike ergometer.

Countries

Denmark

Outcome results

None listed

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