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Beta2-mimetic and Central Nervous System

Beta2-mimetic and Central Nervous System: Effects of Salbutamol on Cortical Excitability and Cerebral Activation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02925130
Acronym
BETACTIV
Enrollment
15
Registered
2016-10-05
Start date
2016-10-31
Completion date
2017-09-28
Last updated
2017-10-02

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

Conditions

Adrenergic Beta-2 Agonist Effect, Albuterol Effect

Brief summary

Beta2-mimetics such as Salbutamol have been shown to have ergogenic effects. Acute and chronic inhaled or oral doses of Salbutamol have been shown to increase whole body exercise and muscle performances. The underlying mechanisms are however unclear. Some data suggest that Salbutamol may have some effects on the central nervous system which may explain the improved exercise and neuromuscular performances. The present study aims to assess the effects of acite inhaled or oral Salbutamol intake on the neuromuscular system by using neurostimulation techniques and magnetic resonance imaging.

Detailed description

The effects of Salbutamol intake will be assessed by using transcranial magnetic stimulation on one hand and magnetic resonance imaging on the other hand. Maximal voluntary activation and cerebral activation will be measured during motor tasks performed until exhaustion after acute inhaled slabutamol intake, acture oral salbutamol intake or oral placebo intake.

Interventions

DRUGSalbutamol

Acute intake of Albuterol, a beta2-mimetic, either inhaled or oral.

DRUGPlacebo

Acute oral intake of a placebo drug

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects without respiratory and cordiovascular diseases * Male * Age between 18 and 35 * Trained subjects (\>6 hours of physical activity per week) * Non- or ex-smoker (smoking cessation since at least 1 year)

Exclusion criteria

* Respiratory, cardiovascular and metabolic diseases * Neuromuscular diseases * thyrotoxicosis, or diabetes treated with insulin * alcoholism * MRI contraindication * TMS contraindication

Design outcomes

Primary

MeasureTime frameDescription
Maximal voluntary activationMeasured immediatly after treatment intake (within 1 h)Measurement performed by using transcranial magnetic stimulation, superimposed on submaximal and maximal quadricep contractions

Secondary

MeasureTime frameDescription
Cortical activationMeasured immediatly after treatment intake (within 1 h)Measurement performed by using magnetic resonance imaging and the intensity of the BOLD signal in response to a motor task.
Exercise enduranceMeasured immediatly after treatment intake (within 1 h)Time to exhaustion during the exercise muscle test.

Countries

France

Outcome results

None listed

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