Skip to content

Clinical Research on the Optimal Management of bronchial thermoplasty in the treatment of asthma

Clinical Research on the Optimal Management of bronchial thermoplasty in the treatment of asthma

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16009878
Enrollment
Unknown
Registered
2016-11-16
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

asthma

Interventions

GroupA: BT treatment group:BT treatment +drugs
Group B: drugs treatment group:drugs

Sponsors

Shanghai 10th People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Severe persistent asthma patients, aged = 18 years, male or female; 2. The patients is consistent with 5-6 levels of the National Asthma Education and Prevention Program (NAEPP) Guideline; Patients with prominent symptoms despite the use of stable maintenance therapy (eg. high-dose ICS + LABA); Patients with fatal acute attack usually requiring critical first aid, even though stable in remission; Patients with poor efficacy or intolerant side effects of drug treatments; 3. Can tolerate bronchoscopy; FEV1 = 50-60% of predicted before bronchodilators; 4. If a former smoker, Quit smoking = 1 year, <10 package years; 5. voluntary participate the clinical research and sign on the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with implanted devices, such as pacemakers or nerve stimulators; 2. Patients allergic to the sedatives, anesthetics and other drugs used during bronchoscopy; 3. Patients who received the treatment previously; 4. Patients with the respiratory tract infection when included; Patients in the acute exacerbation of asthma or adjusted the oral dose of glucocorticoids in the past two weeks; 5. Patients with With coagulopathy or oral anticoagulant drugs; 6. Patients with severe cardiovascular disease, insulin-dependent diabetes mellitus, neoplasms, epilepsy, and other poor compliances intolerant to bronchoscopy; 7. Patient with any situations the researchers believe that is not eligible for inclusion.

Design outcomes

Primary

MeasureTime frame
ACQ;AQLQ;

Secondary

MeasureTime frame
FeNO;PEF;FEV1;EC;lgE;

Countries

China

Contacts

Public ContactXIAOLIAN SONG

Shanghai 10th People's Hospital

120021288@QQ.COM+86 15000766684

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026