Skip to content

The effetcs of asthma medicine on physical performance in athletes

The effects of high dose beta2-agonists on physical performance in healthy male subjects - Effects of beta2-agonists on healthy subjects

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2012-002804-42-DK
Enrollment
9
Registered
2012-09-10
Start date
2012-09-10
Completion date
Unknown
Last updated
2013-07-29

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

Conditions

No medical condition will be investigated. To examine the effects of beta2-agonists on aerobic and anaerobic exercise performance.

Interventions

Trade Name: Bricanyl Product Name: Terbutaline Product Code: R03AC03, R03CC03 Pharmaceutical Form: Inhalation powder Pharmaceutical form of the placebo: Inhalation powder Route of administration of th

Sponsors

Bispebjerg Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: -Sex: Male -Age: 18-40 -Physically active -Informed consent Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 9 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range 0

Exclusion criteria

Exclusion criteria: -Respiratory diseases -Smoker -Asthma -Heart disorders -Exercise-induced bronchoconstrition defined as a post-exercise drop in FEV1 > 10% following an incremental bicycle test to exhaustion. -Allergy towards the study medicine (Bricanyl, Ventolin, Lactose)

Design outcomes

Primary

MeasureTime frame
Main Objective: To examine the effects of beta2-agonists on aerobic and anaerobic exercise performance in healthy subjects.;Secondary Objective: To investigate potassium kinetics in skeletal muscle of healthy subjects.;Primary end point(s): Increased muscle strength, sprint ability and submaximal exercise performance.;Timepoint(s) of evaluation of this end point: 1,5 years

Secondary

MeasureTime frame
Secondary end point(s): Potassium kinetics;Timepoint(s) of evaluation of this end point: 1,5 years

Countries

Denmark

Contacts

Public ContactBispebjerg Hospital

Bispebjerg Hospital Lungemedicinsk forskningesenhed

anderskalsen@gmail.com+4520723113

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026