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临床试验/NCT03109392
NCT03109392已完成2 期

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 个研究点 分布在 1 个国家目标入组 1,050 人开始时间: 2017年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
1,050
试验地点
1
主要终点
Patient-rated intensity of cough on a visual analog scale (VAS)

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

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

排除标准

  • 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

研究组 & 干预措施

Nebulized lignocaine

Experimental

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

干预措施: Nebulized Lignocaine (Drug)

Lignocaine spray

Experimental

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

干预措施: Lignocaine spray (Drug)

Combined spray and nebulization

Active Comparator

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

干预措施: Combined spray and nebulization (Drug)

结局指标

主要结局

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

时间窗: 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.

次要结局

  • 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)

研究者

发起方
Post Graduate Institute of Medical Education and Research, Chandigarh
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ritesh Agarwal

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

Post Graduate Institute of Medical Education and Research, Chandigarh

研究点 (1)

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