跳至主要内容
临床试验/NCT01691963
NCT01691963撤回不适用

Epiglottic Downfolding During Endotracheal Intubation - An Alternative Technique to Improve Glottic Exposure and Facilitate Intubation?

Catharina Ziekenhuis Eindhoven2 个研究点 分布在 1 个国家开始时间: 2013年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
2
主要终点
The Cormack and Lehane grade

研究概览

简要总结

Usually videolaryngoscopy using a videolaryngoscope with a classic Macintosh design is performed with the blade in the vallecula and the epiglottis elevated from the vocal cords indirectly, as in direct laryngoscopy. However, during an audit of videolaryngoscopic practice we noticed that, in obtaining the best view, clinicians frequently and inadvertently advanced the blade into the vallecula to get a better view, such that the epiglottis was downfolded and elevated directly from the vocal cords. However, a better view does not necessarily lead to higher intubation success.

In this randomized, controlled trial, we want to determine the efficacy of videolaryngoscope-guided tracheal intubation using an alternative position for the blade in patients with normal airways.

详细描述

Anaesthesia will be induced in the conventional matter. For patients randomized to the intervention group, when the anaesthesiologist considers the depth of anaesthesia to be sufficient, a C-MAC® videolaryngoscope (Karl Storz, Tuttlingen, Germany), will be placed into the patients mouth. The best possible view of the vocal cords will be obtained with the blade positioned normally in the vallecula anterior to the epiglottis. The epiglottis will be elevated from the vocal cords indirectly, identical with direct laryngoscopy. After this, the best possible view of the vocal cords will be obtained with the blade positioned alternatively in the vallecula posterior to the epiglottis, such that the epiglottis is downfolded and elevated directly from the vocal cords. Views will be scored in both positions using the Cormack and Lehane classification system. When correct laryngoscope positioning can't be achieved with a size 3 blade, a size 4 blade will be used.

For patients not randomized to the intervention group, anaesthesia will also be induced in the conventional matter. When the anaesthesiologist considers the depth of anaesthesia to be sufficient, a C-MAC® videolaryngoscope (Karl Storz, Tuttlingen, Germany), will be placed into the patients mouth. The best possible view of the vocal cords will be obtained with the blade positioned normally in the vallecula anterior to the epiglottis. The epiglottis will be elevated from the vocal cords indirectly, identical with direct laryngoscopy. The view will be scored in this position using the Cormack and Lehane classification system. After this, the patient will be intubated.

Patients will be interviewed 2 and 24 hours postoperatively about sore throat, dysphonia, dysphagia and coughing.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

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

入选标准

  • Informed patient consent
  • ASA I-III
  • Age > 18 years
  • Elective surgery, other than head and/or neck surgery
  • Elective surgery, duration < 1 hour in supine position
  • Pre-operative Mallampati I-II-III

排除标准

  • No informed patient consent
  • Age < 18 years
  • Preoperative complaints of sore throat, dysphagia, dysphonia and coughing
  • Emergency surgery, surgery of head and/of neck
  • Surgery during > 1 hour in other than supine position
  • Locoregional anaesthesia
  • Preoperative Mallampati IV
  • Known difficult airway
  • Bad dentition
  • Dental crowns and/or fixed partial denture
  • Risk of aspiration (fasted < 6 hours, gastroesophageal reflux)

结局指标

主要结局

The Cormack and Lehane grade

时间窗: Patients will be followed for the duration of induction of anaesthesia, an average of 10 minutes

The Cormack and Lehane grade scored in both positions of the C-MAC® videolaryngoscope and consequent success of intubation

次要结局

  • Use of adjuncts(Patients will be followed for the duration of induction of anaesthesia, an average of 10 minutes)
  • Discomfort(Patients will be followed for 24 hours postoperatively)

研究者

发起方
Catharina Ziekenhuis Eindhoven
申办方类型
Other
责任方
Principal Investigator
主要研究者

Barbe Pieters

Principal investigator

Catharina Ziekenhuis Eindhoven

研究点 (2)

Loading locations...

相似试验