Follow-up of Mild Eosinophilic Asthma

NCT04650503 | Unknown

• 1 other identifier: CÉR21799
• Study Type: observational
• Target: 80
• Locations: 1 country
• Sites: 1

Brief Summary

Asthma is a chronic respiratory disease affecting approximately 10% of the population, the majority of patients with very mild to mild asthma. Asthma is characterized primarily by the presence of symptoms clinical variables, reversible airway obstruction and airway hyperresponsiveness. Inflammation is a key factor in the pathophysiology of the disease. Eosinophilic inflammation is the most common type. However, in the literature it is usually associated with more severe and difficult to control asthma. Although mortality associated with asthma has drastically decreased in recent years, several events still occur. Strangely enough, these frequently affect mild asthmatics. Although there is still a misunderstanding in relation to these events, the most recent practice guides have recommended an approach based on the use of inhaled corticosteroids (ICS) in all, including mild asthmatics. This change of therapeutic cap is still debated, but indicates a need for new studies in this population. Recently, the investigators demonstrated that a subgroup of asthma patients with mild asthma had a eosinophilia. The evolution of this subgroup without bronchial obstruction or respiratory symptoms remains unknown. Indeed, it seems imperative to determine the fate of these subjects in comparison with asthma mild non-eosinophilic since it could be a subgroup at risk of poor outcome. The objective of this study will be to examine the course of asthma in very mild to mild asthma patients who exhibit eosinophilic inflammation of the respiratory tract compared to noneosinophilic subjects. This will be a prospective observational, longitudinal study. Participants for whom a result of induced sputum showing an eosinophil level greater than or equal to 3% was observed at least 1 year ago will be contacted to participate in the study. They will be matched for age, gender and duration of asthma to subjects without eosinophilia. These subjects will not be on bronchial anti-inflammatory medication. They will have a complete evaluation including respiratory function tests, a methacholine challenge and sputum induction. They will also complete questionnaires on controlling their asthma and exacerbations.

Conditions

Asthma

Outcome Measures

Primary Outcomes (1)

• Mean annual change in pre bronchodilator forced expiratory volume in one second (FEV1) and FEV1/forced vital capacity (FVC) between baseline and follow-up between the two groups

  calculated using: (initial value - follow-up value)/number of years between the two tests

  At least one year post baseline

Secondary Outcomes (6)

• Clinical sub score of the Asthma Control Scoring system (ACSS) at follow-up between the two groups

  At least one year post baseline

• Number of asthma exacerbations in the year preceding follow-up visit between the two groups

  At least one year post baseline

• Airway reactivity at follow-up between the two groups

  At least one year post baseline

• Prescribed therapy at follow-up between the two groups

  At least one year post baseline

• Airway inflammation between the two groups at follow-up

  At least one year post baseline

Study Arms (2)

Patients with eosinophilic asthma at baseline

Patients showing ≥3% sputum eosinophils at baseline

Other: No intervention

Patients with non eosinophilic asthma at baseline

Patients showing \<3% sputum eosinophils at baseline

Other: No intervention

Interventions

No intervention OTHER

No intervention

Patients with eosinophilic asthma at baseline; Patients with non eosinophilic asthma at baseline

Eligibility Criteria

• Age: 18 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Asthmatic subjects with at least two sputum cell differential results \> 1 year before follow-up visit

You may qualify if:

• With a proven diagnosis of asthma
• With very mild or mild asthma at the time of previous assessment
• With at least two sputum cell differential counts \> 1 year before follow-up visit
• With stable asthma and asthma medication for at least 4 weeks before baseline assessment and before follow-up visit
• Able and willing to consent to study procedures

You may not qualify if:

• Conditions that could affect measurements, such as any active chronic or systemic inflammatory disease, not related to the respiratory system.
• Subjects with a main diagnosis of eosinophilic granulomatosis with polyangiitis (Churg- Strauss syndrome) or hypereosinophilic syndrome.
• Respiratory tract infection in the 4 weeks preceding past assessments and in the 4 weeks preceding follow-up visit.
• Asthma exacerbation in the 4 weeks preceding past assessments in the 4 weeks preceding follow-up visit.
• Current smokers. Ex-smokers must not have smoked for a minimum of 12 months, and should not have a smoking history ≥10 pack years. Subjects who administer nicotine in other forms (patches, chew tobacco, electronic cigarettes, etc.) will also be excluded from the study;
• Concomitant disease or condition which could interfere with the conduct of the study, or for which the treatment might interfere with the conduct of the study, or which would, in the opinion of the investigator, pose an unacceptable risk to the subject in this study, including, but not limited to, cancer, alcoholism, drug dependency or abuse, or psychiatric disease.
• Pregnant or lactating women at the time of follow-up visit.

Sponsors & Collaborators

• Laval University: lead
• GlaxoSmithKline: collaborator

Study Sites (1)

Louis-Philippe Boulet

Québec, G1V4G5, Canada

RECRUITING

MeSH Terms

Conditions

Asthma

Condition Hierarchy (Ancestors)

Bronchial Diseases; Respiratory Tract Diseases; Lung Diseases, Obstructive; Lung Diseases; Respiratory Hypersensitivity; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• Louis-Philippe Boulet, MD

  IUCPQ-UL

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Louis-Philippe Boulet, MD

CONTACT

4186564747; lpboulet@med.ulaval.ca

Marie-Eve Boulay, MSc

CONTACT

4186568711; marie-eve.boulay@criucpq.ulaval.ca

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: October 14, 2020
• First Posted: December 2, 2020
• Study Start: August 1, 2019
• Primary Completion: September 1, 2021
• Study Completion: December 1, 2021
• Last Updated: December 2, 2020

Record last verified: 2020-12

Locations

CA (1)