Status:

UNKNOWN

Mechanisms of Adverse Effects of Long-Acting Beta-Agonists in Asthma

Lead Sponsor:

Imperial College London

Collaborating Sponsors:

European Research Council

Conditions:

Asthma

Eligibility:

All Genders

18+ years

Phase:

PHASE4

Brief Summary

This study aims to elucidate the pathophysiological mechanisms underlying the adverse effects associated with the use of long-acting beta-agonists (LABAs) in asthma. Participants with mild asthma will...

Detailed Description

The use of long-acting beta-agonists (LABAs) alone to treat asthma has been associated with increased mortality rates. Between 2012 and 2013, 3% of patients who died from asthma in the UK were found t...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA
  • Age \> 18 years
  • A doctor's diagnosis of asthma (mild in severity)
  • No current regular asthma treatment or regular asthma treatment in the preceding 6 weeks; only a history of using short-acting bronchodilator inhalers on demand is allowed
  • Pre-bronchodilator FEV1 value \> 70% of the predicted value
  • EXCLUSION CRITERIA
  • History or evidence of chronic respiratory disease other than asthma
  • History or evidence of other disease, blood test results outside the normal reference range or medication use that would impair the ability of participants to safely undertake the study or the ability of researchers to interpret the study results; this includes, but is not limited to, the use of anticoagulants (e.g. warfarin), adenosine diphosphate (ADP) receptor inhibitors (e.g. clopidogrel), antiretroviral therapy (due to the potential for interaction with fluticasone), certain antifungal agents (due to the potential for interaction with fluticasone) and beta-blockers
  • Current use or use in the last 6 weeks of systemic or nasal topical steroids, inhaled corticosteroids or systemic immunosuppressants
  • Platelet count \< 150 x 109/L or international normalised ratio (INR) \> 1.5
  • History of smoking \> 5 pack years, current smoker or history of smoking in the last 4 weeks
  • Current vaping or history of vaping in the last 4 weeks
  • Current illicit drug use/abuse
  • Abnormal chest x-ray appearance
  • Signs or symptoms of upper respiratory tract infection or lower respiratory tract infection in the preceding 6 weeks
  • Cardiac conduction abnormalities on electrocardiogram (ECG)
  • Current pregnancy or planning to become pregnant during the study period
  • Breastfeeding during the study period
  • Inability to provide informed consent to participate in the study
  • Current involvement in any other clinical research studies involving medicinal products or devices; or involvement in clinical research studies involving medicinal products within the last 30 days or within 5 half-lives of the medicinal product (whichever is longer)
  • Inability to speak English or inability to understand verbal or written English
  • Inability to attend hospital for all scheduled study visits
  • Hypersensitivity to any of the investigational medicinal products (IMPs) or their excipients

Exclusion

    Key Trial Info

    Start Date :

    July 23 2021

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ESTIMATED

    End Date :

    September 30 2024

    Estimated Enrollment :

    24 Patients enrolled

    Trial Details

    Trial ID

    NCT04503460

    Start Date

    July 23 2021

    End Date

    September 30 2024

    Last Update

    April 25 2023

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    St Mary's Hospital, Imperial College Healthcare NHS Trust

    London, United Kingdom, W2 1NY