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临床试验/jRCT1042200060
jRCT1042200060已完成不适用

Comparison of double-lumen endobronchial tube and a combination of LMA ProSeal and bronchial blocker for video assisted thoracoscopic surgery: a randomized controlled trial

未提供0 个研究点目标入组 100 人开始时间: 2020年11月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Treatment Purpose
盲法
Single Blind

入排标准

年龄范围
20age old over 至 85age old not(—)
性别
All

入选标准

  • (1) Patients undergoing thoracoscopic lung surgery (including robotic-assisted surgery) for clinical stage I lung cancer under general anesthesia
  • (2) ASA PS (American Society of Anesthesiologists Physical Status) 1 to 3
  • (3) Patients for whom written consent has been obtained from the individual

排除标准

  • (1) Patients undergoing emergency surgery
  • (2) Patients after tracheotomy
  • (3) Patients who are intubated preoperatively
  • (4) Patients with a history of intrathoracic surgery on the operative side
  • (5) Patients with a history of intrathoracic lesions on the operative side and expected adhesions
  • (6) Patients with anticipated tumor invasion of the bronchial tubes or vessels.
  • (7) Patients with an anatomical abnormality that makes normal isolated lung ventilation difficult, such as a tracheal bronchus
  • (8) Patients who undergo a procedure that cannot be managed with normal isolated lung ventilation, such as surgery on the left and right main bronchus.
  • (9) Patients who are expected to have difficulty in securing their airway
  • (10) Patiwnts with severe obstructive ventilatory disturbance (1-second rate <50%)
  • (11) Patients who are allergic to the drug to be used
  • (12) Patients with obvious hoarseness or sore throat preoperatively
  • (13) Patients who are expected to have difficulty in postoperative communication due to dementia, sequelae of cerebrovascular disease, etc.
  • (14) Patients who are judged by the research group to be inappropriate

结局指标

主要结局

-

Incidence of hoarseness on postoperative days 1, 2, and 3

次要结局

  • Incidence of hoarseness and sore throat at the time of PACU exit(at the time of PACU exit)
  • Incidence of sore throats on postoperative days 1, 2, and 3(postoperative days 1, 2, and 3)
  • Degree of sore throat with VAS on postoperative day 1(postoperative day 1)
  • Time to complete lung collapse
  • Quality of surgical field and lung collapse
  • Time to secure the airway
  • Incidence of intraoperative respiratory management problems(intraoperative)
  • Incidence of pneumonia, air leaks from the thoracic draine, unexpected ICU admission, airway injuries, number of days of thoracic drain insertion, and other perioperative complications(perioperative)

研究者

发起方
未提供

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