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| Name | Class |
|---|---|
| Nottingham University Hospitals NHS Trust | OTHER |
| University Hospitals, Leicester | OTHER |
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The purpose of this study is to determine whether an inhaled steroid with a small particle size can be an additional treatment option in patients with refractory eosinophilic asthma.
We have identified a group of patients with refractory asthma who have ongoing eosinophilic airway inflammation despite high dose inhaled corticosteroids.
Traditional inhaled steroids have a relatively proximal airway distribution which may lead to inadequate treatment of the distal airways.
We aim to demonstrate that a steroid inhaler with a smaller particle size which targets the distal airways can be a useful additional treatment option in this group of patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ciclesonide | Active Comparator | Ciclesonide 320 microgrammes twice daily |
|
| Placebo | Placebo Comparator | Placebo 2 inhalations twice daily |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ciclesonide | Drug | Inhaled ciclesonide 320mcg twice daily |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in sputum eosinophil count over the trial period | Sputum will be processed for a differential cell count, with the primary outcome the difference in sputum eosinophil count between active and placebo groups at 8 weeks | 0 weeks (start), 8 weeks (finish) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in alveolar nitric oxide level over the trial period | alveolar nitric oxide has been shown to correlate with eosinophil count on BAL samples. Measured by measuring exhaled nitric oxide at multiple flow rates. | 0 weeks (start), 4 weeks, 8 weeks (finish) |
| Change in bronchial nitric oxide level |
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Inclusion Criteria:
Age 18-80
ACQ >1.5 or a requirement for oral steroids twice a year or more
High dose inhaled steroid (>1000mcg BDP or equivalent)
Treatment with or unsuccessful trial of:
Sputum eosinophil count >3% despite high dose inhaled steroid or >2% with serum eosinophils >0.4x10exp9/l
Clinical response to 2 weeks of oral prednisolone: (any one)
Exclusion Criteria:
Current smoker, or ex-smoker for <12 months
Current treatment with an extrafine steroid inhaler
Respiratory infection within the last 4 weeks
Pregnancy or lactation
Poor compliance with usual asthma medication
Clinical diagnosis of significant bronchiectasis
Use of a medication which may interact with ciclesonide:
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| Name | Affiliation | Role |
|---|---|---|
| Tim Harrison | University of Nottingham | Principal Investigator |
| Ian Pavord | University Hospitals, Leicester | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospitals of Leicester NHS Trust | Leicester | Leicestershire | LE3 9QP | United Kingdom | ||
| Nottingham University Hospitals NHS Trust |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25858909 | Derived | Hodgson D, Anderson J, Reynolds C, Meakin G, Bailey H, Pavord I, Shaw D, Harrison T. A randomised controlled trial of small particle inhaled steroids in refractory eosinophilic asthma (SPIRA). Thorax. 2015 Jun;70(6):559-65. doi: 10.1136/thoraxjnl-2014-206481. Epub 2015 Apr 9. |
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| ID | Term |
|---|---|
| D001249 | Asthma |
| D011657 | Pulmonary Eosinophilia |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| ID | Term |
|---|---|
| D001982 | Bronchial Diseases |
| D008173 | Lung Diseases, Obstructive |
| D012130 | Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
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| ID | Term |
|---|---|
| C120481 | ciclesonide |
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| Placebo | Drug | Matched placebo inhaler two inhalations twice daily |
|
Measured by single flow exhaled nitric oxide at 50 ml/s |
| 0 weeks (start), 4 weeks, 8 weeks (finish) |
| Change in prebronchodilator FEV1 | Prebronchodilator FEV1 and FVC will be recorded with a Vitalograph Wedge Bellows spirometer | 0 weeks (start), 4 weeks, 8 weeks (finish) |
| Change in Juniper Asthma Control Questionnaire (ACQ) score | UK English Version 2001 | 0 weeks (start), 4 weeks, 8 weeks (finish) |
| Change in Juniper Asthma Quality of Life Questionnaire (AQLQ) score | Self-administered United Kingdom Version 1994 | 0 weeks (start), 4 weeks, 8 weeks (finish) |
| Use of oral steroid over the trial period | Dose and duration of any additional oral corticosteroid will be documented | 0-8 weeks |
| Number of patients with adverse events as a measure of safety and tolerability | Adverse events will be recorded throughout the trial period | 0-8 weeks |
| Nottingham |
| Nottinghamshire |
| NG5 1PB |
| United Kingdom |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
| D017681 | Hypereosinophilic Syndrome |
| D004802 | Eosinophilia |
| D007960 | Leukocyte Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |