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Not yet recruiting NCT07150689

Outcome of Bronchoscopy in FB Aspiration

No phase Interventional Foreign Body Aspiration

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rigid bronchoscopy, Flexible scope, Combined Flexible-Rigid Bronchoscopy, Imaging-Guided Bronchoscopy.
Who it may be relevant to
Registry conditions: Foreign Body Aspiration. Basic parameters: 1 Day — 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Assessment of Outcome of Bronchoscopy in Pediatric Patients With Suspected Foreign Body Aspiration Attending at Assiut University Children Hospital

Overview

Outcome of Bronchoscopy in Pediatric patient with foreign body aspiration

Interventions

  • Procedure Rigid bronchoscopy
    Participants will undergo rigid bronchoscopy under general anesthesia using an age-appropriate rigid bronchoscope. The airway will be systematically inspected. Any identified foreign body will be removed using appropriate retrieval devices (optical forceps, retrieval basket, suction). Post-removal, the airway will be re-examined to confirm clearance and detect trauma.
  • Procedure Flexible scope
    Participants will undergo flexible fiberoptic bronchoscopy under sedation or general anesthesia. The bronchoscope will be inserted transorally or transnasally. The airway will be inspected, and foreign body retrieval attempted using retrieval baskets, forceps, or cryoprobe
  • Procedure Combined Flexible-Rigid Bronchoscopy
    Initial flexible bronchoscopy will be performed to locate the foreign body and inspect distal airways, followed by rigid bronchoscopy for definitive removal.
  • Procedure Imaging-Guided Bronchoscopy
    Participants will undergo pre-procedure high-resolution CT or virtual bronchoscopy. Based on imaging, either rigid or flexible bronchoscopy will be performed, targeting the suspected location to reduce procedure time.

Primary outcome measures

  • Rate of Successful Foreign Body Removal [Time frame: During bronchoscopy procedure (intra-operative, within 24 hours of intervention).]
Secondary outcome measures (1)
  • Incidence of procedure-related complications (within 24 hours). [Time frame: Intra-procedure and up to 24 hours post-procedure.]

Eligibility criteria

Inclusion criteria

  • children less than 18 years with suspected foreign body aspiration

Exclusion criteria

  • children with congenital airway anomalies other than foreign body aspiration

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07150689 · FB bronchoscopy

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗