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临床试验/CTRI/2024/04/066317
CTRI/2024/04/066317招募中3 期

A Prospective Randomised Controlled Trial To Compare The Stability Of Bronchial Blocker Between Extraluminal And Intraluminal Placement In Adult Thoracic Surgery - NI

Tata memorial Centre Mumbai0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Patients who are deemed suitable for both extraluminal as well as intraluminal placement of BB by a thoracic anaesthetist. This would typically include patients in whom a cuffed single lumen endotracheal tube of size 7.5 or above is considered appropriate i.e. most male patients and female patients with height above 155 cm
  • 2.Patients in whom a bronchial blocker with a fixed angle tip is chosen for lung isolation e.g. Coopdech blocker, Tappa blocker or Fuji blocker

排除标准

  • 1.Patients with risk of cross contamination of lung with blood or infected secretions, or those with bronchopleural fistula
  • 2.Patients in whom EZ or Arndt blocker is used for lung isolation
  • 3.Patients with abnormal tracheobronchial anatomy detected on radiological imaging or flexible bronchoscopy
  • 4.Patients with an anticipated difficult airway
  • 5.Patients with unanticipated difficult airway e.g. those requiring more than 3 attempts at endotracheal intubation, those requiring rescue measures to maintain oxygenation, etc
  • 6.Patients belonging to ASA III physical status
  • 7.Patients at high risk of regurgitation and aspiration
  • 8.Patients in whom a 7F BB is unable to achieve a seal (and therefore isolation)
  • 9.Patients who cannot give valid consent
  • 10.Pregnancy

研究者

发起方
Tata memorial Centre Mumbai

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