A study to compare and assess a new technique to remove foreign material in respiratory tract in children through bronchoscopy

A Comparative Evaluation of a Novel Technique for Bronchoscopy Guided Tracheobronchial Foreign Body Removal in Children-A Randomised Controlled Trial

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/03/018061

Enrollment

Registered

2019-03-13

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: X58- Exposure to other specified factors

Interventions

Intervention1: 2ml of 2% lignocaine(nebulization) and 1 ml of 2% plain lignocaine(transtracheal block): Nebulization will be done with 2ml of 2% xylocaine for 10-15 minutes prior to bronchoscopy. Afte

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA grade I to II 2.Recent H/O of tracheobronchial foreign body aspiration 3.Parents giving consent for participation in the study

Exclusion criteria

Exclusion criteria: 1.Bronchoscopy through tracheostomy 2.Anterior neck swelling 3.Known allergy to local anesthetics 4.Renal, hepatic, or cardiovascular dysfunction, neurological disorders 5.Mental retardation or delayed milestones 6.Suspected coagulopathy 7.Parents refusal to participate in the study

Design outcomes

Primary

Measure	Time frame
1.To compare the effect on intra-procedure and post-procedure hemodynamics (Heart Rate, Non-Invasive Blood Pressure) and oxygen saturation. 2.Total dose of propofol used during procedure in both the groups. 3.Post-procedure recoveryTimepoint: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.	—

Measure

Time frame

1.To compare the effect on intra-procedure and post-procedure hemodynamics (Heart Rate, Non-Invasive Blood Pressure) and oxygen saturation. 2.Total dose of propofol used during procedure in both the groups. 3.Post-procedure recoveryTimepoint: Heart rate,Non-invasive blood pressure and saturation will be recorded continuously every 3 minutes throughout the procedure and till return of consciousness.

—

Secondary

Measure	Time frame
To look for complications encountered in such procedures like airway intervention, bronchospasm, laryngospasm, vocal cord injury and laryngeal or subglottic odema in both groups.Timepoint: Complications noted from start of bronchoscopy till completion of procedure and return of consciousness every 5 minutes	—

Countries

India

Contacts

Public ContactRicha Rai

Institute of Medical Sciences-Banaras Hindu University

richasgpgi@gmail.com9452516982

Outcome results

None listed

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