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Outcome of Bronchoscopy in FB Aspiration

A

Assiut University

Status

Not yet enrolling

Conditions

Foreign Body Aspiration

Treatments

Procedure: Combined Flexible-Rigid Bronchoscopy
Procedure: Rigid bronchoscopy
Procedure: Imaging-Guided Bronchoscopy
Procedure: Flexible scope

Study type

Interventional

Funder types

Other

Identifiers

NCT07150689
FB bronchoscopy

Details and patient eligibility

About

Outcome of Bronchoscopy in Pediatric patient with foreign body aspiration

Enrollment

75 estimated patients

Sex

All

Ages

1 day to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • children less than 18 years with suspected foreign body aspiration

Exclusion criteria

  • children with congenital airway anomalies other than foreign body aspiration

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

75 participants in 4 patient groups

Rigid Bronchoscopy
Active Comparator group
Description:
Standard of care in most pediatric centers; performed under general anesthesia to visualize and remove FB. Gold standard for both diagnosis and treatment
Treatment:
Procedure: Rigid bronchoscopy
Flexible Bronchoscop
Experimental group
Description:
Flexible scope used for diagnosis and sometimes removal (especially in distal airways or when FB is small). Evaluate if less invasive flexible bronchoscopy can be effective.
Treatment:
Procedure: Flexible scope
Combined Approach
Experimental group
Description:
Initial flexible bronchoscopy for diagnosis and airway inspection, followed by rigid bronchoscopy for removal if needed. Compare efficiency and safety of combined method.
Treatment:
Procedure: Combined Flexible-Rigid Bronchoscopy
Imaging-Guided Approach
Experimental group
Description:
High-resolution CT or virtual bronchoscopy first; bronchoscopy only if imaging suggests FB. Assess if imaging can reduce unnecessary bronchoscopies.
Treatment:
Procedure: Imaging-Guided Bronchoscopy

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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