Overview
Concentrations of Formoterol in Blood and Urine
Status:
Unknown status
Unknown status
Trial end date:
2010-12-01
2010-12-01
Target enrollment:
0
0
Participant gender:
Male
Male
Summary
The purpose of the study is to assess the blood and urine concentrations of inhaled formoterol.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Bispebjerg HospitalCollaborator:
Hormone Laboratory, Aker University Hospital, Oslo, NorwayTreatments:
Formoterol Fumarate
Criteria
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 allergy.
- Allergy towards the study medicine.
- Use of beta-2-agonist 10 days prior to study day.