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Nebulized Lignocaine for Topical Airway Anesthesia During Flexible Bronchoscopy: A Randomized Controlled Trial

Not Applicable
Completed
Conditions
Bronchopulmonary Disease
Interventions
Drug: Saline Nebulization
Registration Number
NCT03040193
Lead Sponsor
All India Institute of Medical Sciences, New Delhi
Brief Summary

Flexible bronchoscopy is one of the most widely performed procedures for diagnosis of various bronchopulmonary diseases. Most patients tolerate the procedure well although cough is often reported as a distressing symptom. It is likely that the acceptance of bronchoscopy would be significantly improved with control of cough. Use of sedation during bronchoscopy has been reported to improve procedure tolerance. However, awake(no sedation) bronchoscopy is routinely performed at many centres including ours.

Topical lignocaine is administered during bronchoscopy for local anaesthesia. There is limited literature on the efficacy of lignocaine delivered with the nebulized route during awake flexible bronchoscopy. This study would help to determine the utility of nebulized lignocaine in airway anaesthesia during flexible bronchoscopy.

Detailed Description

For all patients meeting the inclusion criteria, the demographic profile including age, sex, weight, smoking history and the type of procedures performed during bronchoscopy shall be recorded. A written informed consent will be obtained from all participants. The patients who undergo flexible bronchoscopy would be randomised in a one is to one ratio either to nebulized lignocaine (4%) or saline (placebo) nebulization group. Prior to the bronchoscopy blood pressure, pulse rate, respiratory rate and pulse oximetry saturation will be recorded at the baseline Patients in both the groups shall be prepared in a similar fashion except for the nebulized lignocaine. Patient, Operator, outcome assessor will be blinded to the allocation.

During the procedure, 1.5ml aliquots of 1% lignocaine will be delivered through the bronchoscope using spray-as-you go technique. The patients would be monitored for any adverse effects throughout the procedure. The bronchoscopist doing the procedure will be provided 2 VAS charts to mark the severity of cough and overall procedure satisfaction.

Post procedure, patients will record the pain experienced while undergoing the procedure on the faces pain rating scale.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Adult (Age > 18 years) patients undergoing diagnostic or therapeutic flexible bronchoscopy
Exclusion Criteria
  1. Pregnancy
  2. Hypoxemia (oxygen saturation [by pulse oximetry] < 92% with Fio2 of ≥ 0.3
  3. Bronchoscopy done through endotracheal or tracheostomy tube
  4. Not willing to provide informed consent.
  5. Patient requiring sedation for flexible bronchoscopy
  6. Patients with known allergy to lignocaine -

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Nebulized LignocaineLignocaine Nebulization4% Lignocaine administered as nebulization for topical anaesthesia during bronchoscopy procedure
Nebulized SalineSaline NebulizationNormal Saline administered as nebulization for topical anaesthesia during bronchoscopy procedure
Primary Outcome Measures
NameTimeMethod
Operator rated overall procedure satisfaction VASAt study completion approx. 12 months
Operator rated cough VASAt study completion approx. 12 months
Secondary Outcome Measures
NameTimeMethod
Total dose of Lignocaine administered (mg)At study completion approx. 12 months
Number of patients receiving dose >8.2mg/KgAt study completion approx. 12 months

Trial Locations

Locations (1)

All India Institute of Medical Sciences

🇮🇳

New Delhi, India

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