Step-down of Inhaled Corticosteroids (ICS) in Non-eosinophilic Asthmatics
Primary Purpose
Asthma
Status
Completed
Phase
Phase 4
Locations
Belgium
Study Type
Interventional
Intervention
Step-down
Sponsored by
About this trial
This is an interventional treatment trial for Asthma focused on measuring Non-eosinophilic Asthma, Inhaled corticosteroids, Step-down
Eligibility Criteria
Inclusion Criteria:
- At least 18 years of age
- Physician-diagnosed asthma based on the presence of typical symptoms (wheezing, breathlessness, chest tightness, cough)
Asthma confirmed by:
- Forced expiratory volume in 1 second (FEV1) increase of at least 12% and 200 mL after inhalation of 400 mcg salbutamol
- And/or a provocative concentration of methacholine causing a 20% fall in FEV1 (PC20M) less than 16 mg/ml
- Sputum eosinophils rate less than 3%
- Absolute blood eosinophils count less than 400 per mm3
- Treatment with a stable dose of inhaled corticosteroid (ICS) for the previous three months
Exclusion Criteria:
High risk of asthma-related death, defined by:
- Near-fatal asthma history, requiring a stay in an intensive care unit
- Current using or recent discontinuation (four weeks) of oral corticosteroids (OCS)
- Treatment with omalizumab
- Pregnant women
Sites / Locations
- University Hospital of Liege
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Step-down
Arm Description
Step-down of the inhaled corticosteroid (ICS) dose
Outcomes
Primary Outcome Measures
Percentage of patients meeting the success criterion at each visit until the end of the study (corresponding to a discontinuation of the treatment by inhaled corticosteroids (ICS) for 6 months)
The success criterion is defined at each visit as:
- An Asthma Control Questionnaire (ACQ) score lower than 1.5 or a variation of the ACQ score from baseline smaller than 0.5
AND
- A number of severe exacerbations from the start of the step-down smaller or equal to the number of severe exacerbations in the previous year
Secondary Outcome Measures
Evolution of the number of severe exacerbations, defined as use of systemic corticosteroids during at least 3 days or hospitalizations or emergency visits due to asthma with use of systemic corticosteroids
Evolution of the frequency of self-reported adverse event of inhaled therapy for asthma
Evolution of treatment compliance measured by the Mediation Adherence Report Scale (MARS) and by pharmacy records
Evolution of the asthma control measured by the Asthma Control Questionnaire (ACQ)
Evolution of the asthma control measured by the Asthma Control Test (ACT)
Evolution of the asthma related quality of life by the mini-Asthma Quality of Life Questionnaire (miniAQLQ)
Evolution of the Fractional Exhaled Nitric Oxide (FeNO)
Evolution of lung function measured by percentage of predicted Forced Expiratory Volume in 1 second (%FEV1)
Evolution of lung function measured by Forced Expiratory Volume in 1 second (FEV1) divided by Forced Vital Capacity (FVC)
Evolution of lung function measured by reversibility to Short Acting Beta2-Agonists (SABA)
Evolution of inflammatory blood markers : blood cell count, fibrinogen, C-Reactive Protein (CRP)
Evolution of sputum markers of inflammation : rates of neutrophils, eosinophils, macrophages, lymphocytes, epithelial cells
Evolution of the number of moderate exacerbations, defined as the number of visits to an emergency room, the number of unscheduled doctor or pneumologist visits, and increases in reliever use
Evolution of the score of ICQ-S ("Inhaled Corticosteroids side-effect Questionnaire")
Check of the inhalation technique
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02169323
Brief Title
Step-down of Inhaled Corticosteroids (ICS) in Non-eosinophilic Asthmatics
Official Title
Step-down of Inhaled Corticosteroids (ICS) in Non-eosinophilic Asthmatics
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
June 2014 (undefined)
Primary Completion Date
February 27, 2017 (Actual)
Study Completion Date
February 27, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Renaud Louis
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
There is growing evidence that non-eosinophilic asthmatics are less sensitive to inhaled corticosteroids (ICS) than eosinophilic asthmatics.
As non-eosinophilic asthmatic patients are treated by ICS according to international guidelines for asthma, the investigators would like to investigate whether stepping-down of ICS in these patients may be safe. Indeed, the investigators can reasonably expect that a progressive cessation of ICS is possible in some of these patients without any clinical worsening.
Detailed Description
For patients whose asthma is not controlled at the beginning of the study, a step-up of the treatment is planned to the step 4 of Global Initiative for Asthma (GINA). This step-up will last for 3 months and will permit to ensure that these patients achieve the best possible level of asthma control. A progressive step-down of the inhaled corticosteroids (ICS) will then be achieved.
For patients whose asthma is controlled at the beginning of the study, a progressive step-down of the ICS will be directly achieved.
The progressive step-down of the ICS dose will be undertaken every 3 months according to the dose levels defined by GINA guidelines (from high to low daily dose) until a complete cessation of the ICS for 6 months. Other associated asthma treatment of asthma will be kept unchanged.
At each quarterly visit, a clinical composite outcome will be measured, for each patient. This composite outcome includes the score of asthma control questionnaire (ACQ) and the number of exacerbations. This outcome will determine at each visit if patients continue the study (success criterion) or stop the study (failure criterion). The success criterion is defined in the section "Current Primary Outcome"
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Non-eosinophilic Asthma, Inhaled corticosteroids, Step-down
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Step-down
Arm Type
Experimental
Arm Description
Step-down of the inhaled corticosteroid (ICS) dose
Intervention Type
Other
Intervention Name(s)
Step-down
Intervention Description
Step-down of the inhaled corticosteroid (ICS) dose until discontinuation for 6 months
Primary Outcome Measure Information:
Title
Percentage of patients meeting the success criterion at each visit until the end of the study (corresponding to a discontinuation of the treatment by inhaled corticosteroids (ICS) for 6 months)
Description
The success criterion is defined at each visit as:
- An Asthma Control Questionnaire (ACQ) score lower than 1.5 or a variation of the ACQ score from baseline smaller than 0.5
AND
- A number of severe exacerbations from the start of the step-down smaller or equal to the number of severe exacerbations in the previous year
Time Frame
Up to 12 months to reach a 6 month stop of ICS
Secondary Outcome Measure Information:
Title
Evolution of the number of severe exacerbations, defined as use of systemic corticosteroids during at least 3 days or hospitalizations or emergency visits due to asthma with use of systemic corticosteroids
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the frequency of self-reported adverse event of inhaled therapy for asthma
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of treatment compliance measured by the Mediation Adherence Report Scale (MARS) and by pharmacy records
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the asthma control measured by the Asthma Control Questionnaire (ACQ)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the asthma control measured by the Asthma Control Test (ACT)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the asthma related quality of life by the mini-Asthma Quality of Life Questionnaire (miniAQLQ)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the Fractional Exhaled Nitric Oxide (FeNO)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of lung function measured by percentage of predicted Forced Expiratory Volume in 1 second (%FEV1)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of lung function measured by Forced Expiratory Volume in 1 second (FEV1) divided by Forced Vital Capacity (FVC)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of lung function measured by reversibility to Short Acting Beta2-Agonists (SABA)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of inflammatory blood markers : blood cell count, fibrinogen, C-Reactive Protein (CRP)
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of sputum markers of inflammation : rates of neutrophils, eosinophils, macrophages, lymphocytes, epithelial cells
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the number of moderate exacerbations, defined as the number of visits to an emergency room, the number of unscheduled doctor or pneumologist visits, and increases in reliever use
Time Frame
Every 3 months during the study (up to 15 months)
Title
Evolution of the score of ICQ-S ("Inhaled Corticosteroids side-effect Questionnaire")
Time Frame
Every 3 months during the study (up to 15 months)
Title
Check of the inhalation technique
Time Frame
Every 3 months during the study (up to 15 months)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least 18 years of age
Physician-diagnosed asthma based on the presence of typical symptoms (wheezing, breathlessness, chest tightness, cough)
Asthma confirmed by:
Forced expiratory volume in 1 second (FEV1) increase of at least 12% and 200 mL after inhalation of 400 mcg salbutamol
And/or a provocative concentration of methacholine causing a 20% fall in FEV1 (PC20M) less than 16 mg/ml
Sputum eosinophils rate less than 3%
Absolute blood eosinophils count less than 400 per mm3
Treatment with a stable dose of inhaled corticosteroid (ICS) for the previous three months
Exclusion Criteria:
High risk of asthma-related death, defined by:
Near-fatal asthma history, requiring a stay in an intensive care unit
Current using or recent discontinuation (four weeks) of oral corticosteroids (OCS)
Treatment with omalizumab
Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Renaud Louis, MD-PhD
Organizational Affiliation
University of Liege
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Liege
City
Liege
ZIP/Postal Code
4000
Country
Belgium
12. IPD Sharing Statement
Citations:
PubMed Identifier
29383782
Citation
Demarche S, Schleich F, Henket M, Paulus V, Louis R, Van Hees T. Step-down of inhaled corticosteroids in non-eosinophilic asthma: A prospective trial in real life. Clin Exp Allergy. 2018 May;48(5):525-535. doi: 10.1111/cea.13106. Epub 2018 Mar 6.
Results Reference
derived
Learn more about this trial
Step-down of Inhaled Corticosteroids (ICS) in Non-eosinophilic Asthmatics
We'll reach out to this number within 24 hrs