Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06066606

U-LABA/ICS Effects on Exercise Performance, Vilanterol

Physiological Response to U-LABA/ICS With Emphasis on Exercise Performance, Vilanterol

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Morten Hostrup, PhD · Academic / Other
Sex
All
Age
18 Years – 39 Years
Healthy volunteers
Accepted

Summary

The purpose of the project is to investigate exercise performance in humans following bronchodilation induced by acute inhalation of beta2-agonist vilanterol + fluticasone furoate

Conditions

Interventions

TypeNameDescription
DRUGVilanterol and Fluticasone Furoate (low dose)Participants are administered 25 µg of vilanterol + fluticasone furoate
DRUGVilanterol and Fluticasone Furoate (high dose)Participants are administered 100 µg of vilanterol + fluticasone furoate
DRUGPlaceboParticipants are administered placebo

Timeline

Start date
2023-10-03
Primary completion
2026-07-15
Completion
2026-12-01
First posted
2023-10-04
Last updated
2025-04-10

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT06066606. Inclusion in this directory is not an endorsement.