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临床试验/KCT0006618
KCT0006618已完成未知

Comparison of high flow nasal cannula and conventional nasal cannula during sedation for endoscopic submucosal dissection: a randomized controlled trial

Samsung Medical Center0 个研究点目标入组 64 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
64

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19?(Year) 至 o Limit(—)
性别
All

入选标准

  • ASA physical status I to III
  • Patients undergoing endoscopic submucosal dissection

排除标准

  • - Patients under the age of 18
  • - Patients requiring oxygen therapy
  • - Patients unable to breathe through the nasal
  • - Patients with severe impaired coagulation profile or who may have nasal bleeding
  • - Patients who have developed or worsened congestive heart failure within the last 6 months
  • - Patients with increased intracranial pressure
  • - Patients with ASA class IV or higher
  • - Patients with unstable hemodynamics
  • - Patients with a history of pneumothorax
  • - Patients with oral and nasal infections
  • - Pregnant or lactating women
  • - Patients who do not understand this study and who refuse the study
  • - Patients with a history of serious psychological disease

研究者

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