U-LABA/ICS Effects on Exercise Performance, Indacaterol
Launched by MORTEN HOSTRUP, PHD · Sep 27, 2023
Trial Information
Current as of July 27, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how a medication called indacaterol, combined with mometasone furoate, affects exercise performance in physically active adults. The researchers want to see if using this medication can help improve how well people can exercise after taking it. The trial is currently looking for participants aged 18 to 39 who are very active, exercising more than five hours a week and have a high level of oxygen consumption during exercise.
To be eligible for the study, you should not have severe asthma or certain heart conditions, and you should not be pregnant, a smoker, or have donated blood in the last three months. If you qualify and decide to participate, you can expect to undergo some tests to assess your exercise performance and overall health. This trial is a great opportunity for those who are active and want to contribute to research that could help improve exercise capabilities for other 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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Copenhagen, Dk, Denmark
Patients applied
Trial Officials
Morten Hostrup, PhD
Principal Investigator
University of Copenhagen
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported