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Concentrations of Salmeterol in Blood and Urine

B

Bispebjerg Hospital

Status and phase

Unknown
Phase 4

Conditions

Asthma

Treatments

Drug: inhaled salmeterol

Study type

Interventional

Funder types

Other

Identifiers

NCT00914901
SAL2009JE
EudraCT number 2009-012069-70

Details and patient eligibility

About

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

Full 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.

Enrollment

30 estimated patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

30 participants in 3 patient groups

Healthy
Other group
Description:
10 healthy men
Treatment:
Drug: inhaled salmeterol
Asthmatics
Other group
Description:
10 male asthmatic subjects
Treatment:
Drug: inhaled salmeterol
Elite athletes with asthma
Other group
Description:
10 male elite athletes with asthma
Treatment:
Drug: inhaled salmeterol

Trial contacts and locations

1

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Central trial contact

Jimmi Elers, MD

Data sourced from clinicaltrials.gov

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