Skip to content

A Study of the Efficacy and Safety of Bronchoscopic Airway Clearance and Amphotericin B Spraying in Patients With ABPA

A Prospective, Multicenter, Observational Cohort Study on the Efficacy and Safety of Bronchoscopic Airway Clearance and Amphotericin B Spraying in Patients With Allergic Bronchopulmonary Aspergillosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07362667
Enrollment
44
Registered
2026-01-23
Start date
2026-01-10
Completion date
2028-12-31
Last updated
2026-01-23

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

Conditions

ABPA, Airway Clearance, Allergic Bronchopulmonary Aspergillosis, Allergic Bronchopulmonary Aspergillosis (ABPA), Amphotericin B, Bronchoscope, Mucus Plug

Keywords

Allergic Bronchopulmonary Aspergillosis, ABPA, Amphotericin B, bronchoscope, Airway Clearance, mucus plug

Brief summary

To evaluate the efficacy and safety of bronchoscopic airway clearance and amphotericin B spraying in the treatment of allergic bronchopulmonary aspergillosis

Interventions

PROCEDUREThe patients were treated with bronchoscopic airway clearance and amphotericin B spraying

In addition to standard medical therapy (oral glucocorticoids with or without oral antifungal agents), bronchoscopic airway clearance and bronchoscopic spraying of amphotericin B (depending on the effectiveness of bronchoscopic mucus plug removal, At least one time of bronchoscopic airway clearance and amphotericin B spraying). The previous treatment for bronchial asthma was maintained, including inhaled corticosteroids + long-acting β-receptor agonists, leukotriene receptor antagonists, etc.

Sponsors

Qianfoshan Hospital
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. Meet the diagnostic criteria of allergic bronchopulmonary aspergillosis, according to the ISHAM guidelines for the diagnosis and treatment of allergic bronchopulmonary aspergillosis (2024 revision), and the presence of mucus plugs or hyperattenuated mucus confirmed by chest high-resolution CT (HRCT). 2. Active disease: Newly diagnosed allergic bronchopulmonary aspergillosis or an acute exacerbation after discontinuation of treatment (defined as a \> 14 day history of clinical worsening or radiographic progression of allergic bronchopulmonary aspergillosis and a ≥50% increase in total serum IgE from the last recorded value during the stable phase, excluding other causes of the acute exacerbation) in patients with previously diagnosed allergic bronchopulmonary aspergillosis. 3. Age ≥ 18 years old.

Exclusion criteria

1. Allergic bronchopulmonary aspergillosis - serotype (i.e., meets the diagnostic criteria for allergic bronchopulmonary aspergillosis, but chest CT shows no obvious abnormality); 2. Patients with absolute or relative contraindications to electronic bronchoscopy; 3. Known history of allergy to amphotericin B or any of its excipients; 4. Patients with bronchiectasis caused by human immunodeficiency virus infection, active tuberculosis, pulmonary malignant tumor or other non-allergic bronchopulmonary aspergillosis; 5. Combined with other diseases requiring long-term systemic use of glucocorticoids or immunosuppressants (such as autoimmune diseases); 6. Patients with previous or current smoking history; 7. Pregnant or lactating women; 8. Currently participating in other interventional clinical research; 9. Any other conditions considered by the investigator to preclude participation in the study (e.g., nonadherence, predicted survival \<1 year, or severe mental illness that prevented cooperation).

Design outcomes

Primary

MeasureTime frameDescription
Radiographic response rate after 4 months of treatment4 monthsRadiographic remission: defined as the removal of mucus plugs in the airway on radiographic examination
Immunological remission rate after 4 months of treatment4 monthsImmunological remission: defined as at least a 50% decrease in total serum IgE from baseline
The remission rate of clinical symptoms after 4 months of treatment4 monthsClinical symptom relief: The semi-quantitative rating of clinical symptoms was evaluated using Likert scores with at least 50% improvement in symptoms

Secondary

MeasureTime frameDescription
psychological Scale (Hospital Anxiety and Depression Scale, HADS)2 years
Aspergillus fumigatus sIgE2 years
Number of acute exacerbations within 1 year of drug withdrawal after 4 months of treatment1 year
Number of acute exacerbations within 2 years after 4 months of treatment2 years
Treatment response rate at 8 weeks8 weeks
Number of hospitalizations due to acute exacerbations of allergic bronchopulmonary aspergillosis2 years
Time from discontinuation to first exacerbation2 years
Quality of life score (AQLQ or mini-AQLQ)2 years
After drug withdrawal, the number of patients who achieved treatment remission2 yearsThe remission phase was defined as sustained (\>6 months) clinical-radiologic improvement in the absence of (or discontinuation of) glucocorticoid therapy and the absence of an increase in total serum IgE of 50% or more from the last recorded value during the stable phase
Serum total IgE2 years
All-cause mortality2 years

Countries

China

Contacts

CONTACTQian Qi, Dr.
qiqianqlh@163.com+86 13706380314

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026