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Pharmacological effects of acute and accumulated salbutamol in relation to doping analysis

Pharmacological effects of acute and accumulated salbutamol in relation to doping analysis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2016-002819-18-DK
Enrollment
20
Registered
2016-09-05
Start date
2016-12-14
Completion date
Unknown
Last updated
2019-11-25

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

Conditions

Pharmacological effects of acute and accumulated salbutamol in relation to doping analysis

Interventions

Trade Name: Ventoline Product Name: Ventoline Pharmaceutical Form: Oral solution INN or Proposed INN: SALBUTAMOL SULFATE CAS Number: 510

Sponsors

Bispebjerg University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: • Male and female aged 18-45 years • Physical active, at least 2 times a week • VO2-max at least 45 ml/min/kg (women) and 50 ml/min/kg (men) • Non-smokers • No daily use of medicine 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 20 F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range 0

Exclusion criteria

Exclusion criteria: Hypersensitivity towrads the active substance or any one of the other substances within the medicine. Coronary heart desiease, asthma or other cronical disease Not able to get doctors permission to participate in the trial after an objective examination Pregnancy

Design outcomes

Primary

MeasureTime frame
Main Objective: The aim is to investigate the pharmaco dynamics and kinetics for acute and accumulated salbutamol in relation to doping analysis;Secondary Objective: Not applicable; Primary end point(s): Urine concentrations of salbutamol Performance test (wingate) ;Timepoint(s) of evaluation of this end point: Spring 2019

Secondary

MeasureTime frame
Secondary end point(s): Not applicable;Timepoint(s) of evaluation of this end point: Not applicable

Countries

Denmark

Contacts

Public ContactMorten Hostrup

Bispebjerg University Hospital

mortenhostrup@gmail.com

Outcome results

None listed

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