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Corticosteroid

Fluticasone for Asthma (EATA Trial)

N/A
Waitlist Available
Led By Louis-Philippe Boulet, MD
Research Sponsored by Laval University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years

Summary

* The inflammatory process that leads to the development of asthma may be present before the onset of asthma symptoms and cause a certain degree of airway hyperresponsiveness. Without treatment it may induce irreversible airway structural changes that are associated with permanent changes in airway functions, persistent airway hyperresponsiveness and lead to the development of asthma symptoms. * Atopic subjects with asymptomatic airway hyperresponsiveness and first degree relatives with a history of asthma are at higher risk to develop symptomatic asthma. Early treatment of airway inflammation in these predisposed subjects with " borderline " or mild airway hyper-responsiveness could prevent the development of asthma symptoms, and reduce or even normalize airway responsiveness. * In very mild asthmatic subjects (bronchodilator need \< thrice a week), early anti-inflammatory treatment can lead to " normalisation " or airway responsiveness in a significant number of subjects and prevent the need for subsequent regular therapy. This is particularly true for those showing blood/sputum eosinophilia. Objectives: To compare perception of bronchoconstriction, pulmonary function and airway inflammation in subjects with mild symptomatic asthma and asymptomatic asymptomatic airway hyperresponsiveness Methods: To compare the influence of inhaled fluticasone propionate 250 mcg/day for 3 months followed by 100 mcg/day for 9 months on airway inflammation and methacholine responsiveness in a double-blind, placebo-controlled, parallel groups study including non-smoking atopic subjects with mild asthma and asymptomatic airway hyperresponsiveness

Eligible Conditions
  • Asthma
  • Bronchial Hyperreactivity
  • Bronchial Hyperresponsiveness

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

Trial Design

1Treatment groups
Placebo Group
Group I: PlaceboPlacebo Group1 Intervention
Placebo inhalator will be used by subjects in the placebo group(same course as patients in the treated group)

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Who is running the clinical trial?

Laval UniversityLead Sponsor
430 Previous Clinical Trials
178,312 Total Patients Enrolled
23 Trials studying Asthma
3,140 Patients Enrolled for Asthma
Louis-Philippe Boulet, MDPrincipal InvestigatorHôpital Laval
23 Previous Clinical Trials
3,575 Total Patients Enrolled
18 Trials studying Asthma
3,060 Patients Enrolled for Asthma
~3 spots leftby Oct 2025