Inhaled Corticosteroids on Airway Smooth Muscle in Asthma
Primary Purpose
Asthma
Status
Withdrawn
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
budesonide
Sponsored by

About this trial
This is an interventional basic science trial for Asthma focused on measuring asthma, airway smooth muscle, inhaled corticosteroids
Eligibility Criteria
Inclusion Criteria:
- Physician diagnosis of asthma
- Age 18-60
- Intermittent asthma symptoms < once/week
- FEV1>80% of predicted
- Not on inhaled corticosteroid therapy
Exclusion Criteria:
- Previous long-term use of inhaled corticosteroids (within 1 year of entry into study)
- Past history of hypersensitivity to budesonide
- Current smokers, or less than 3 years since quitting smoking
- Less than 4 weeks from an exacerbation
- On steroid-sparing agent or immunosuppressant such as azathioprine, methotrexate and ciclosporin
- Concomitant anti-IgE therapy
- Pregnancy
- Previous bronchoscopy within three months of this study
Sites / Locations
- Asthma lab, Royal Brompton Hospital, Sydney Street
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
overall
Arm Description
Outcomes
Primary Outcome Measures
Changes in ASM mass, proliferation and migration after ICS therapy; changes in chemokine release after ICS therapy
Secondary Outcome Measures
Changes in sub-basement membrane thickness and inflammatory cell count after ICS therapy
Full Information
NCT ID
NCT00661973
First Posted
April 16, 2008
Last Updated
September 12, 2019
Sponsor
Imperial College London
Collaborators
Royal Brompton & Harefield NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT00661973
Brief Title
Inhaled Corticosteroids on Airway Smooth Muscle in Asthma
Official Title
The Effect of Inhaled Corticosteroids (ICS) on Airway Smooth Muscle in Asthma
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Withdrawn
Why Stopped
The study was withdrawn for administrative reasons
Study Start Date
April 2008 (Actual)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
March 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London
Collaborators
Royal Brompton & Harefield NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main objective is to evaluate how treatment with inhaled corticosteroids (ICS) affects the characteristics of airway smooth muscle (ASM) cells from asthmatic subjects. Our hypothesis is that airway smooth muscle cell dysfunction plays an important role in the pathogenesis of asthma, and that treatment with inhaled corticosteroids reverses the abnormalities in airway smooth muscle cell function.
Detailed Description
Aims and Objectives
Most of the work published to date on the effect of steroids on ASM has been carried out in animal models or in in vitro experiments. We would like to evaluate in vivo whether abnormalities in ASM function respond to ICS. Because ASM cells can be obtained from bronchial biopsies obtained via bronchoscopy, we will examine endobronchial biopsies from corticosteroid-naïve, mild asthmatic subjects. In particular, we will examine whether ICS have any effect ASM mass, proliferation and expression of different contractile proteins (α-actin and myosin) and chemokines, and will assess in vitro the response of ASM cells to stimulation by TGF-β and IL-1β. We will also examine the effect of dexamethasone on chemokine release and induced proliferation in vitro before and after treatment with ICS.
We will examine the effect of inhaled corticosteroids in 12 subjects with mild asthma. The subjects will be studied during a baseline period and again after receiving treatment with inhaled corticosteroid therapy with Budesonide Turbohaler (400 ug bd) for 4 weeks. The results of these two periods will be compared.
There will be 5 study visits. In the first two visits, the subjects will undergo spirometry with reversibility testing, a methacholine challenge test, skin prick tests and IgE levels, measurement of exhaled nitric oxide, and subjects will complete an Asthma Control Questionnaire and an Asthma Quality of Life Questionnaire. The third visit will be the day admission for the bronchoscopy. They will be given asthma control diary cards to complete during the 4-week treatment with ICS and receive their ICS turbohaler. At visit 4, they will have repeat spirometry and methacholine challenge to assess if there has been a change secondary to treatment with ICS. The final visit will be for the second bronchoscopy, when the dairy card and ICS inhaler will be collected, and the subjects will complete the Asthma Control and Quality of Life questionnaire.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
asthma, airway smooth muscle, inhaled corticosteroids
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
overall
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
budesonide
Other Intervention Name(s)
pulmicort
Intervention Description
inhaled budesonide (turbohaler) 400 micrograms twice a day for 4 weeks
Primary Outcome Measure Information:
Title
Changes in ASM mass, proliferation and migration after ICS therapy; changes in chemokine release after ICS therapy
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Changes in sub-basement membrane thickness and inflammatory cell count after ICS therapy
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Physician diagnosis of asthma
Age 18-60
Intermittent asthma symptoms < once/week
FEV1>80% of predicted
Not on inhaled corticosteroid therapy
Exclusion Criteria:
Previous long-term use of inhaled corticosteroids (within 1 year of entry into study)
Past history of hypersensitivity to budesonide
Current smokers, or less than 3 years since quitting smoking
Less than 4 weeks from an exacerbation
On steroid-sparing agent or immunosuppressant such as azathioprine, methotrexate and ciclosporin
Concomitant anti-IgE therapy
Pregnancy
Previous bronchoscopy within three months of this study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kian F Chung, MBBS FRCP MD DSc
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Asthma lab, Royal Brompton Hospital, Sydney Street
City
London
ZIP/Postal Code
SW3 6NP
Country
United Kingdom
12. IPD Sharing Statement
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Inhaled Corticosteroids on Airway Smooth Muscle in Asthma
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