Nocturnal TLA for Severe Allergic Asthma After Withdrawal of Omalizumab Therapy
Study Details
Study Description
Brief Summary
This is a randomized, controlled study with a 48-week treatment phase to determine the clinical efficacy of temperature controlled laminar flow device (TLA, Airsonett™) in the patients with severe allergic asthma who are withdrawal of omalizumab therapy
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This is a randomized, controlled study with a 48-week treatment phase to determine the clinical efficacy of temperature controlled laminar flow device (TLA, Airsonett™) in the patients with severe allergic asthma who are withdrawal of omalizumab therapy. All patients will be recruited from outpatient clinics of Thoracic Department of Chang Gung Memorial Hospital and meet the inclusion criteria. After entry the study, these patients will continuous their concomitant asthma medicines, except the treatment of omalizumab. These patients will be randomized (1:1) to receive TLA device or matching Control group. The participants will be recorded by randomized number to protect their private information. To minimize a potential treatment group imbalance of clinical asthma management practice and concomitant asthma medication use, randomization will be stratified by concomitant asthma medication [in addition to inhaled corticosteroid (ICS) and long-acting β2-agonist (LABA)] use at baseline: (1) patients not receiving theophylline, oral β2-agonists, antileukotrienes or maintenance oral steroids; (2) patients receiving one or more from theophylline, oral β2-agonists and anti-leukotrienes, but not receiving maintenance oral steroids; (3) patients receiving maintenance oral steroids. The doses of ICS and LABA (taken separately or as a fixed combination) and other concomitant asthma medications will be kept constant through the treatment period. If they have asthma exacerbation of emergency visit or/and hospitalization, or > or =2 episodes of asthma exacerbation (defined as a worsening of asthma symptoms requiring treatment with systemic corticosteroids), the patients either with TLA or Control group will return to start the omalizumab therapy till the end of 48-week follow-up. Omalizumab dose is based on the patient's body weight and total serum immunoglobulin E (IgE) level at screening and is administered every 2 or 4 weeks to provide a dose of at least 0.016 mg/kg per IU/ml of IgE. Patients are permitted short-acting β2-agonist rescue medication as required.
Patients make study visits at weeks 0, 2, 4, 12, 24, 36 and 48 of the treatment phase. The primary efficacy variable is the first time to asthma exacerbations during the 48-week TLA treatment phase. Rate of hospitalization, and emergency visit per year will be also recorded. Diary cards are used to record the clinical symptom score, asthma control test (ACT) and use of rescue medication in the internet of Asthma Help.
Quality of life will be assessed using the Sino-Nasal Outcome Test (SNOT-22) score at weeks 0, 12, 24, 36 and 48 of the treatment phase. Spirometry and exhaled NO will be performed at each visit. All visits include assessment of vital signs and physical examination.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: TLA device These patients will be withdrawal of omalizumab treatment and receive nocturnal temperature controlled laminar flow device at nighttime for 12 months. |
Device: Nocturnal Temperature Controlled Laminar Flow Device
Record of the time to first asthma exacerbation, lung function and exhaled NO level
|
| Placebo Comparator: None device These patients will be withdrawal of omalizumab treatment and do not receive TLA device for 12 months. |
Other: None Device
Record of the time to first asthma exacerbation, lung function and exhaled NO level
|
Outcome Measures
Primary Outcome Measures
- The first time of asthma exacerbation [Through study completion of 48 weeks]
Time to the first significant asthma exacerbation or ER visit or hospitalization will be also recorded.
Secondary Outcome Measures
- Spirometry [at 0, 4, 12, 24, 36, and 48 weeks after enrollment]
Pulmonary function testing, including FVC and FEV1
- Exhaled nitric oxide [at 0, 4, 12, 24, 36, and 48 weeks after enrollment]
measured level is ppb.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Willing to sign a written consent form
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Male and female subjects were diagnosed severe allergic asthma and received omalizumab as add-on therapy for more 4 than months and had stable asthma control.
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Men and women over the age of 20 and less than 80 year-old
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Accept application of TLA or not after withdrawal of omalizumab therapy
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Positive reaction of specific IgE (Phadiatop) for one or more than on indoor allergens.
Exclusion Criteria:
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Having an exacerbation within 4 weeks before entry the study
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Using immunosuppressants within 3 months of the first visit
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Having recent upper airway infection or systemic corticosteroid usage within 4 weeks
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Bronchiectasis
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Active pulmonary tuberculsis
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COPD
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Cystic fibrosis
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Chang Gung Memorial Hospital | Taoyuan | Taiwan |
Sponsors and Collaborators
- Chang Gung Memorial Hospital
Investigators
- Principal Investigator: Chun-Hua Wang, MD, Department of Thoracic Medicine, Chang Gung Memorial Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 201600573A3