Clinical Trial

Flexible Bronchoscopy in Resistant Pneumonia in PICU

Study acronym: FFP-RP PICU
Completed
View on ClinicalTrials.gov →
Summary
Pneumonia remains a leading cause of morbidity and mortality among critically ill children admitted to Pediatric Intensive Care Units (PICUs). A proportion of patients fail to demonstrate clinical or radiological improvement despite receiving at least five days of appropriate broad-spectrum antibiotic therapy, a condition commonly referred to as resistant or non-resolving pneumonia. These patients often require further diagnostic evaluation to identify persistent infection, resistant microorganisms, airway abnormalities, or alternative diagnoses. Flexible fiberoptic bronchoscopy (FFB) with bronchoalveolar lavage (BAL) is an important diagnostic procedure that permits direct visualization of the tracheobronchial tree and collection of lower respiratory tract specimens for microbiological analysis. The findings obtained through FFB may identify the underlying etiology of persistent pulmonary disease and guide subsequent therapeutic decisions. This observational study aims to evaluate the diagnostic yield, clinical utility, safety, and impact of flexible fiberoptic bronchoscopy with bronchoalveolar lavage in children with resistant pneumonia admitted to the Pediatric Intensive Care Unit at Abu El-Reesh Children's Hospital, Cairo University. Eligible patients are children who demonstrate persistent clinical and radiological evidence of pneumonia despite receiving at least five days of appropriate first-line broad-spectrum antibiotic therapy. Clinical characteristics, bronchoscopic findings, microbiological results, bronchoalveolar lavage cultures, molecular diagnostic results, treatment modifications, procedure-related complications, and clinical outcomes will be analyzed. The findings of this study are expected to provide evidence regarding the role of flexible bronchoscopy in the diagnostic evaluation and management of resistant pneumonia in critically ill pediatric patients.
Protocol Amendment History 4 changes
critical Trial completed 2026-07-21
notable Enrollment increased: 58 -> 70 participants 2026-07-21
notable Primary completion moved earlier: 2026-04-01 -> 2025-06-29 2026-07-21
minor Completion moved earlier: 2026-04 -> 2025-08-03 2026-07-21
Trial Details
NCT Number NCT07421440
Lead Sponsor Mansour Gomaa Mohammed Saleh
Conditions Pneumonia, Resistant Pneumonia, Resistant Pneumonia in Critically Ill Pedaitric Patients
Enrollment 70 participants
Start Date 2023-02-05
Primary Completion 2025-06-29 (estimated)
Study Completion 2025-08-03 (estimated)
Updated on ClinicalTrials.gov 2026-07-20