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Study on the Influencing Factors of Deposition Rate and Mucus Clearance in the Lungs of Patients with Bronchiectasis after Nebulization Administration and Exploration of Its Mechanism Using EIT Technology

Study on the Influencing Factors of Deposition Rate and Mucus Clearance in the Lungs of Patients with Bronchiectasis after Nebulization Administration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100544
Enrollment
Unknown
Registered
2025-04-10
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Bronchiectasis

Interventions

Physiological saline group:The subjects nebulized 18F NaF and underwent PET/CT scanning after nebulization. Each subject underwent EIT examination to determine pulmonary obstructive and compliance.
Compound Ipratropium Bromide Solution for Inhalation+ Saline Group:The subjects first nebulized and inhaled carbidone, then nebulized and inhaled 18F NaF, and after nebulization was completed, PET/CT

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients included in the study must meet all three criteria (1. 2. 3.) and be evaluated by experienced clinical doctors. 1 Age range: 18-75 years old; 2 In terms of imaging, high-resolution CT shows the following direct signs: "signet ring sign" is usually accompanied by bronchial wall thickening, and the ratio of bronchial/concomitant pulmonary artery diameter (B/A>1); From the center to the periphery, the bronchi do not gradually become thinner; Dilated bronchial shadow can be seen within 1 cm from the pleura. Indirect signs: thickening of bronchial wall; Mucous impaction; Mosaic sign or "gas trap" was found on expiratory CT scan; 3 Symptomatically, there are clinical manifestations of chronic cough, purulent sputum, and/or recurrent hemoptysis.

Exclusion criteria

Exclusion criteria: 1 Cannot tolerate salt water atomization; 2 Cannot tolerate lung function tests or pulmonary ventilation imaging examinations; 3 Those who cannot understand the experimental operation process and correctly use experimental instruments; 4 Women who are preparing for pregnancy, pregnant, or breastfeeding; 5 Merge severe systemic diseases and mental abnormalities; Merge malignant tumors, etc 6 Refuse to participate in the experiment.

Design outcomes

Secondary

MeasureTime frame
Obstructive pulmonary disease;

Primary

MeasureTime frame
Total lung uptake value;Total camera value of branch expansion area;Lung compliance;

Countries

China

Contacts

Public Contactlin-ling cheng

The First Affiliated Hospital of Guangzhou Medical University

linling@gird.cn+86 199 2836 2227

Outcome results

None listed

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