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The effect assessment of atomization inhalation therapy used in mucous bronchiectasis

The effect assessment of atomization inhalation therapy used in mucous bronchiectasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15006911
Enrollment
Unknown
Registered
2015-08-10
Start date
2015-08-15
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

bronchiectasis

Interventions

A:atomization inhalation treatment for three month, then oral expectorant drugs for three month
B:oral expectorant drugs for three month then atomization inhalation treatment for three month

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with bronchiectasis, and given priority to bronchiectasis performance,conforms to the diagnosis of bronchiectasis (BE) standard: repeatedly cough, cough with sputum(or) history of hemoptysis. By the high resolution CT diagnosis of bronchiectasis:the airway diameter larger than with pulmonary artery diameter; Bronchial not tapering more than 2 cm; Pleural wall visible bronchial as 1 cm; 2. In bronchiectasis stable period, ranging in age from 18 to 80 years old; No smoking or quit smoking > more than 1 year, sputum volume is more than 10 ml 24 hours a day; 3. Bronchiectasis stable period is defined as: (1) the 24 hours of sputum volume change < 20%; (2) The change of the FEV1 and FVC < 20%; (3) no obvious change in respiratory symptoms; (4) the type and dosage of the drug use without obvious change;The above symptoms last more than three weeks can be diagnosed as Bronchiectasis stable period. 4. The participants agreed to participate in this study, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. With refractory bronchial asthma, active tuberculosis, heart failure, idiopathic pulmonary fibrosis, cystic fibrosis bronchiectasis, pulmonary embolism, disease history and other effects observed indicators; 2. A history of allergic disease; 3. A history of acute and chronic cardiopulmonary kidney tumors; 4. Hard to cooperate with or understand ability is limited, can't cooperate with researchers; 5. The expectorant drug allergies; 6. Patients with pregnancy and lactation; 7. Can't timely follow-up of patients; 8. Rounding out the first 4 weeks had oral/intravenous antibiotics (except Macrolide antibiotics).

Design outcomes

Primary

MeasureTime frame
Sputum volume 24 hours a day;The color of sputum;Leicester Cough Questionnaire(LCQ);induced Sputum cell count;

Secondary

MeasureTime frame
lung function;Sputum viscosity;6 minute walking test;differential cell counts in induced sputum;

Countries

China

Contacts

Public ContactZE GUANG ZHENG
zheng862080@139.com+86 18928868242

Outcome results

None listed

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