Skip to content

Clinical Application of BAL Combined with Microscopic Spraying Inhalation of Sputum Mucus Lysate in the Treatment of Non asthmatic and Refractory Pneumonia in Children

Clinical Application of BAL Combined with Microscopic Spraying Inhalation of Sputum Mucus Lysate in the Treatment of Non asthmatic and Refractory Pneumonia in Children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113319
Enrollment
Unknown
Registered
2025-11-27
Start date
2022-05-17
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Non wheezing refractory pneumonia in children

Interventions

Research Group 1:BAL+Injecting Acetylcysteine Solution for Inhalation under bronchoscopy
Research Group 2:BAL+Injecting Ambroxol Hydrochloride Solution for Inhalation under bronchoscopy
Control Group:BAL

Sponsors

Guangzhou Panyu District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The diagnostic criteria of refractory pneumonia: pneumonia that has not achieved obvious clinical efficacy or ideal results after comprehensive and effective measures have been taken for pulmonary infection is called refractory pneumonia, including (1) some severe pneumonia with poor efficacy, (2) pneumonia that has not been cured for a long time, and (3) pneumonia with slow absorption. Among them: 1) Severe pneumonia refers to severe ventilation and/or gas exchange dysfunction or extrapulmonary complications; 2) Prolonged disease course (> 2 weeks), refractory to active treatment and deterioration; 3) Slow absorption refers to the patients whose symptoms and signs were improved after the use of anti-infective drugs, but the pulmonary pathological examination after 2 weeks showed that the absorption of lesions was less than 50%; 2. Airway foreign body and congenital pulmonary dysplasia were excluded by fiberoptic bronchoscopy; 3. Informed consent was obtained from the parents.

Exclusion criteria

Exclusion criteria: (1) patients with wheezing/wheezing symptoms or signs; (2) severe cardiopulmonary dysfunction; (3) severe arrhythmia; (4) high fever; (5) patients with active hemoptysis; (6) severe hemorrhagic disease; (7) coagulation dysfunction; Severe pulmonary hypertension and may induce massive hemoptysis; (8) patients with severe malnutrition who could not tolerate surgery; (9) allergic to investigational drugs; (10) other serious adverse reactions and complications, which were difficult to continue treatment.

Design outcomes

Primary

MeasureTime frame
Hot annealing time;Lung rale disappearance time;Interleukin-6 ;Interleukin-10;Tumor Necrosis Factor-a;

Secondary

MeasureTime frame
Cluster of Differentiation 3+;Cluster of Differentiation 4+;Cluster of Differentiation 8+;

Countries

China

Contacts

Public ContactCai Jierong

Guangzhou Panyu District Central Hospital

xmg668@163.com+86 138 2449 3238

Outcome results

None listed

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