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临床试验/JPRN-jRCTs052230120
JPRN-jRCTs052230120招募中2 期

Investigational research of an automatic control of vasoactive drug and infusion volume to avoid abnormal hypotension

Matsuki Yuka0 个研究点目标入组 100 人开始时间: 2023年10月27日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
100

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

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1. Male and female patients over 20 years old at the time of informed consent
  • 2. Patients with ASA physical status of 1 and 2 who are scheduled for surgery under general anesthesia
  • 3. Patients who understand the contents of this study and are willing to provide written informed consent for participation in this study

排除标准

  • 1. Patients with a history of hypersensitive to propofol, remifentanil, rocuronium or sugammadex
  • 2. Patients who cannot connected BIS Sensor for placement on the forehead
  • 3. Patients who cannot received rocuronium after first single dose
  • 4. Patients who cannot measured non-invasive sphygmomanometer
  • 5. Patients undergoing surgery with hypothermia
  • 6. Patients undergoing cardiovascular surgery
  • 7. Patients with supraventricular rhythm irregularities such as atrial fibrillation, atrial flutter, or sinus arrhythmia
  • 8. Patients with expected blood loss of 1000 mL or more
  • 9. Pregnant patients or patients having a possibility of pregnancy. Patients who are breast feeding or attempting to become pregnant
  • 10. Pregnant patients or patients having a possibility of pregnancy. Patients who are breast feeding or attempting to become pregnant

研究者

发起方
Matsuki Yuka

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