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Concentrations of Salmeterol in Blood and Urine

Blood and Urinary Concentrations of Inhaled Salmeterol in Asthmatic Subjects and Elite Athletes With Asthma.

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00914901
Enrollment
30
Registered
2009-06-05
Start date
2009-07-31
Completion date
2011-03-31
Last updated
2009-06-05

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

Conditions

Asthma

Keywords

Asthma, Doping, Salmeterol, Beta-agonist, Urine concentrations

Brief summary

The purpose of the study is to assess the blood and urine concentrations of inhaled salmeterol.

Detailed description

The purpose of the study is to assess the serum and urine concentrations of salmeterol after inhalation of 100 microgram salmeterol in one dose. Furthermore, to evaluate any difference in three groups: 10 healthy men, 10 male asthmatic subjects and 10 male elite athletes with asthma.

Interventions

DRUGinhaled salmeterol

Inhalation of 100 micrograms salmeterol in one dose.

Sponsors

Hormone Laboratory, Aker University Hospital, Oslo, Norway
CollaboratorOTHER
Bispebjerg Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Physician-diagnosed asthma with positive reversibility or challenge test. * Informed consent. * Age between 18-45 years. * Sex: male. * Asthma classified as mild to moderate according to GINA guidelines. * Used beta-2-agonist in minimum 12 months.

Exclusion criteria

* Smokers or ex-smokers with a smoking history of 10 pack years or more. * Respiratory tract infections within the last 2 weeks prior to study day. * Subjects with other chronic diseases than asthma and/or allergy. * Allergy towards the study medicine. * Use of beta-2-agonist 10 days prior to study day.

Design outcomes

Primary

MeasureTime frame
Serum and urine concentrations of salmeterolbaseline, 4, 8, and 12 hours after medicine administration

Countries

Denmark

Contacts

Primary ContactJimmi Elers, MD
jele0004@bbh.regionh.dk+45 35313208

Outcome results

None listed

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