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Search / Trial NCT06077019

Role of Lung Function for Exercise Capacity in Well-trained Individuals

Launched by MORTEN HOSTRUP, PHD · Oct 4, 2023

Trial Information

Current as of July 27, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is looking at how different medications may affect exercise performance in physically active individuals. Specifically, the study will explore the impact of inhaling two combinations of medications—vilanterol with fluticasone furoate and indacaterol with mometasone furoate—on how well people can perform during exercise. The goal is to understand how lung function influences exercise capacity in healthy, well-trained adults.

To qualify for this study, participants should be between 18 and 39 years old, exercise regularly (at least 5 hours a week), and have a high level of oxygen consumption. However, those with severe asthma, certain heart problems, significant lung function issues, or who are pregnant or smokers will not be eligible. If you join the study, you can expect to participate in assessments that measure your exercise performance and lung function while using the study medications. This research could provide valuable insights into how to enhance exercise capabilities in fit individuals.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Age 18-39
  • Physically active \> 5 h weekly
  • Maximal oxygen consumption classified as high or very high
  • Exclusion Criteria:
  • 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

About Morten Hostrup, Phd

Dr. Morten Hostrup, PhD, is a distinguished clinical trial sponsor with extensive expertise in advanced research methodologies and a strong focus on innovative therapeutic solutions. With a robust background in clinical pharmacology and biostatistics, Dr. Hostrup has successfully led numerous trials aimed at evaluating the safety and efficacy of novel treatments across various therapeutic areas. His commitment to scientific excellence and regulatory compliance ensures that all clinical studies are conducted with the highest ethical standards, ultimately contributing to the advancement of healthcare and improved patient outcomes.

Locations

Copenhagen, , Denmark

Patients applied

0 patients applied

Trial Officials

Morten Hostrup, PhD

Principal Investigator

University of Copenhagen

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported