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Clinical Trials/NCT03109392
NCT03109392
Completed
Phase 2

A Randomized-controlled Trial to Compare the Effectiveness of 4% Nebulized Lignocaine Versus 10% Lignocaine Spray in Patients Undergoing Flexible Bronchoscopy

Post Graduate Institute of Medical Education and Research, Chandigarh1 site in 1 country1,050 target enrollmentMay 1, 2017

Overview

Phase
Phase 2
Intervention
Nebulized Lignocaine
Conditions
Patients With Indication for Flexible Bronchoscopy
Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Enrollment
1050
Locations
1
Primary Endpoint
Patient-rated intensity of cough on a visual analog scale (VAS)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Flexible bronchoscopy is common procedure used in the diagnosis and treatment of a variety of tracheobronchial diseases. During routine diagnostic flexible bronchoscopy, the most distressing symptom experienced by the patients is a cough, and control of a cough is vital for a successful procedure. The investigators hypothesized that either nebulized lignocaine or lignocaine spray given alone prior to flexible bronchoscopy for inducing topical anesthesia will have similar efficacy compared to the combination of the two agents.

Detailed Description

Flexible bronchoscopy is common procedure used in the diagnosis and treatment of a variety of tracheobronchial diseases. The bronchoscope can be used to sample material not only from the visualized regions but also from the more distal pulmonary parenchyma. It is a safe outpatient exam that carries little risk. While performing the procedure most of the patients express some fear of pain, difficulty in breathing, nasopharyngeal irritation, and cough. During routine diagnostic flexible bronchoscopy, the most distressing symptom experienced by the patients is a cough, and control of a cough is vital for a successful procedure. Administration of a topical anaesthetic drug to the upper airway, larynx, and tracheobronchial tree can reduce a cough and patient's discomfort. The most commonly used topical anaesthetic agent in bronchoscopy is lignocaine because of its quick onset and short duration of action with decreased toxicity as compared to other agents. There are several ways to achieve topical anaesthesia in flexible bronchoscopy including nebulization, direct spray, by tracheal injection, or via nasal, or "spray as you go" technique through the working channel of the bronchoscope. The use of topical anaesthesia, sedation, and analgesia during flexible bronchoscopy varies according to physicians, institutions and geographic locations in the world. Generally, moderate sedation is used in bronchoscopy in which patients can respond to verbal commands. Deep sedation is less commonly used in which patients cannot be easily aroused but respond to repeated or painful stimulation. Antoniades et al. demonstrated that topical lidocaine through the bronchoscope significantly decreased cough frequency and the total dose of sedation required during flexible bronchoscopy. In a randomized controlled trial of 54 patients, Keane et al. concluded that nebulized and sprayed lignocaine have similar efficacy as topical anaesthetics in fiberoptic bronchoscopy but patients preferred the nebulized route. Noitasaeng et.al. concluded in their study that spraying lidocaine took less time to start the procedure, with greater ease of instrumentation, less incidence of hypersecretion, less gag reflex, and smooth operation during the procedure but patients preferred nebulized lidocaine administration. At the investigators' center, it has been a routine practice to perform flexible bronchoscopy without sedation in patients who require only diagnostic flexible bronchoscopy and assessment of airway anatomy and other routine procedures such as endobronchial biopsy or transbronchial biopsy. Previously, the investigators had shown that 1% lignocaine given by spray-as-you-go method was similar in efficacy to 2% lignocaine for topical anesthesia during routine flexible bronchoscopy. However, in this study both the groups received nebulized lignocaine and lignocaine spray prior to flexible bronchoscopy in addition to lignocaine solution ad lib. The investigators hypothesized that either nebulized lignocaine or lignocaine spray given alone prior to flexible bronchoscopy for inducing topical anesthesia will have similar efficacy compared to the combination of the two agents.

Registry
clinicaltrials.gov
Start Date
May 1, 2017
End Date
June 30, 2018
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Post Graduate Institute of Medical Education and Research, Chandigarh
Responsible Party
Principal Investigator
Principal Investigator

Ritesh Agarwal

Consultant, Department of Pulmonary Medicine, Principal Investigator, Clinical Professor

Post Graduate Institute of Medical Education and Research, Chandigarh

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years
  • Willing for flexible bronchoscopy procedure a

Exclusion Criteria

  • Requirement of intravenous sedation to undergo any procedure including EBUS-TBNA, conventional TBNA, radial EBUS procedure and interventional pulmonary procedures
  • Sensitivity to lignocaine
  • Hemodynamically unstable patients (SBP \< 90 mm Hg)
  • Baseline hypoxemia (SpO2 \<92% on room air)
  • Pregnancy
  • Comorbid illness such as heart failure, CKD, chronic liver disease and others
  • Failure to provide informed consent

Arms & Interventions

Nebulized lignocaine

2.5 ml of 4% lignocaine will be administered via nebulization prior to bronchoscopy

Intervention: Nebulized Lignocaine

Lignocaine spray

10 puffs of 10% (10mg/puff) lignocaine spray will be sprayed at 10 seconds intervals into the pharynx immediately prior to bronchoscopy

Intervention: Lignocaine spray

Combined spray and nebulization

Combination of 2.5 ml of 4% lignocaine via nebulization prior to bronchoscopy and 2 puffs of 10% (10mg/puff) lignocaine spray sprayed at 10 seconds intervals into the pharynx immediately prior to bronchoscopy

Intervention: Combined spray and nebulization

Outcomes

Primary Outcomes

Patient-rated intensity of cough on a visual analog scale (VAS)

Time Frame: One hour

The cough VAS is a 100-mm scale anchored by no cough on one end and worst cough on the other; the patient will indicate the severity of a cough by marking a line.

Secondary Outcomes

  • Patient-rated VAS of overall satisfaction of the procedure(One hour)
  • Total lignocaine dose(Immediately following the procedure)
  • Changes in respiratory rate following the procedure(Baseline and 5 minutes after the procedure)
  • Pain assessment by the patient using the faces pain rating scale(One hour)
  • Changes in heart rate following the procedure(Baseline, during and 5 minutes after the procedure)
  • Operator-rated intensity of cough on a VAS(Immediately following the procedure)
  • Changes in blood pressure following the procedure(Baseline and 5 minutes after the procedure)
  • Changes in oxygenation status following the procedure(Baseline, during and 5 minutes after the procedure)
  • Willingness of the patient to undergo the procedure yet again, if required(One hour)
  • Duration of procedure (in minutes)(Immediately following the completion of flexible bronchoscopy)
  • Adverse reactions related to lignocaine(One hour)

Study Sites (1)

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