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China Alair System Registry Study-CARE Study

Registry of Bronchial Thermoplasty (BT) Procedures in China

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02206269
Acronym
CARE
Enrollment
225
Registered
2014-08-01
Start date
2015-04-30
Completion date
2019-06-30
Last updated
2018-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Brief summary

The objective of this Registry is to collect real-world outcome data for bronchial thermoplasty (BT) procedures in patients with severe persistent asthma who remain symptomatic despite taking standard of care maintenance medications.

Detailed description

Data will be used to confirm the impact of BT on safety, effectiveness, quality of life, and the anticipated reduction in healthcare utilization events and cost by way of a reduction in severe asthma exacerbations.

Interventions

The Alair system is used for doing bronchial thermoplasty.

Sponsors

BSC International Medical Trading (Shanghai) Co., Ltd.
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patient is an adult aged 18 years or older with severe persistent asthma who remains symptomatic despite taking standard of care maintenance medications. 2. Patient is able to read, understand, and sign a written Informed Consent to participate in the Registry and able to comply with the study requirements. 3. Patient is able to undergo bronchoscopy in the opinion of the Investigator or per hospital guidelines and as described in the Alair System Directions for Use (DFU).

Exclusion criteria

1. Patient has an implanted electrical stimulation device (e.g., a pacemaker, cardiac defibrillator, or deep nerve or deep brain stimulator). 2. Patient has any other medical condition that would make them inappropriate for study participation, in the Investigator's opinion.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of severe asthma exacerbations following BT with the Alair System.1 yearSevere asthma exacerbation is defined as worsening of asthma symptoms requiring use of systemic corticosteroids (tablets, suspension, or injection) (NAEPP Guidelines, 2007). For patients already taking oral corticosteroids on a daily or alternate day basis, a severe asthma exacerbation is defined as a worsening of asthma symptoms requiring any increase in daily dose of systemic corticosteroids. For consistency, courses of corticosteroids separated by 1 week or more will be treated as separate severe exacerbations.

Secondary

MeasureTime frameDescription
Quarlity of life of Patients1 yearAsthma Quality of Life Questionnaire (AQLQ) score Asthma Control Questionnaire(ACQ)
Health care utilization1 yearEmergency Department Visits,Hospitalizations,Unscheduled office visits including urgent care visits
FEV11 yearPre- and post-bronchodilator FEV1
Serious respiratory adverse events1 yearRates of and proportion of patients with serious respiratory adverse events

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026