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Clinical Trials/NCT03696914
NCT03696914CompletedNot Applicable

Characteristics of the Eosinophilic Asthma Phenotype: an Observational Study in Patients From a Tertiary Care Center With Various Asthma Severities: The Quebec Heart and Lung Institute-Laval University Retrospective Asthma Database Analysis

Laval University1 site in 1 country918 target enrollmentStarted: June 6, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
918
Locations
1
Primary Endpoint
Asthma severity according to medication use

Study Overview

Brief Summary

In asthma, the type and importance of the inflammatory response in the airways has allows identification of different phenotypes. Of these, one of the most common is eosinophilic asthma, based on induced sputum differential cell count. Patients with severe asthma and an eosinophilic asthma phenotype have different pathophysiological characteristics than those seen in patients with with mild asthma. However, few studies have compared patients with eosinophilic phenotype according to the severity of asthma. In addition, the stability of the phenotype based on the sputum results has been criticized.

This study aims to describe the characteristics of patients with eosinophilic asthma phenotype according to the severity of asthma and determine the stability of the phenotype.

Detailed Description

Characteristics of asthmatic subjects with sputum eosinophilia will be compared according to asthma severity.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged 18 years and over
  • With a proven diagnosis of asthma as defined by one of the above criteria of current guidelines (36):
  • Forced expiratory volume in one second (FEV1) increase by at least 12% (and ≥200 ml) after administration of a bronchodilator
  • Current asthma symptoms and a methacholine provocative concentration inducing a 20% fall in FEV1 (PC20) <16 mg/ml
  • A respirologist's current diagnosis of asthma found in the patient's medical report
  • Non-smokers or smokers/ex-smokers defined as someone with a smoking history <10 pack-years
  • With sputum differential cell count result
  • Considered to receive optimal treatment for their disease (as per current guidelines except for patients included in exploratory objective
  • Stable asthma and asthma medication for at least 4 weeks before data analysis
  • Written informed consent obtained for inclusion in the database

Exclusion Criteria

  • Any respiratory disease apart from asthma
  • Current or ex-smokers should not have a smoking history ≥10 pack-year before data analysis. Patients who administer nicotine in other forms (patches, chew tobacco, e-cigarette, etc.) will be excluded
  • Unstable asthma medication <4 weeks before data analysis
  • Asthma exacerbation (see definition below) <4 weeks before data analysis
  • Respiratory tract infection <4 weeks before data analysis

Outcomes

Primary Outcomes

Asthma severity according to medication use

Time Frame: Baseline

Prevalence of patients with 3% or more sputum eosinophils in mild, moderate and severe asthma

Secondary Outcomes

  • FEV1 percent predicted(Baseline)
  • ACSS symptom sub-score(Baseline)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Louis-Philippe Boulet

MD, FRCPC, Respirologist

Laval University

Study Sites (1)

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