U-LABA/ICS Effects on Exercise Performance, Vilanterol
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Exercise Performance
In brief
The purpose of the project is to investigate exercise performance in humans following bronchodilation induced by acute inhalation of beta2-agonist vilanterol + fluticasone furoate
Key facts
- Study ID
- NCT06066606
- Run by
- Morten Hostrup, PhD
- People needed
- 30
- Starts
- 2023-10-03
- Expected to finish
- 2026-12-01
- Last updated by the study team
- 2025-04-10
Who can join
Age: 18 and older, up to 39. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 18-39
- Physically active > 5 h weekly
- Maximal oxygen consumption classified as high or very high
You may not qualify if…
- Diagnosed with severe asthma and been in treatment with long-acting beta2-agonist/corticosteroid
- ECG abnormality
- ACQ score > 1.5
- Severe bronchial hyperreactivity as determined by mannitol test
- FEV1/FVC ratio < 0.7 determined with spirometry
- Chronic illness determined to be a potential risk for participant during study
- In chronic treatment with medication that may interfere with study results
- Pregnancy
- Smoker
- Blood donation during the past 3 months
Where it is running
- August Krogh Building — Copenhagen, DK, Denmark (enrolling)
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.