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临床试验/JPRN-jRCT2090220278
JPRN-jRCT2090220278已完成Unknown

Multicenter comparative study of cardiac output measurement by non-invasive estimated continuous cardiac output (esCCO) and arterial pressure-based cardiac output (APCO) monitoring device in surgery patients under general anesthesia

ihon Kohden Corporation0 个研究点目标入组 60 人开始时间: 2017年2月24日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
60

研究概览

简要总结

esCCO is as a clinically useful CO monitor as APCO, which is well validated.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • Eligible patients were expected to meet all of the following criteria:
  • 1) patients undergoing planned surgery under general anesthesia
  • 2) patients whose surgical operation is expected to last for at least 2 hours
  • 3) patients undergoing surgical operation in the supine posture
  • 4) patients already requiring IBP measurement
  • 5) patients aged 20 years or older at the time of providing informed consent
  • 6) patients having voluntarily provided written consent for participation in this study, based on full understanding after sufficient explanation

排除标准

  • Patients who meet any of the following criteria were excluded from participating in this study.
  • 1) patients having been considered difficult to anesthetise as specified in the Table of Points of Remuneration for Examination and Treatment L008 at preoperative examination
  • 2) patients having been diagnosed to have any of the following findings at preoperative examination:
  • i) supraventricular rhythm irregularities including atrial fibrillation, atrial flutter and sinus arrhythmia
  • ii) bigeminy and trigeminy
  • iii) second- or third-degree atrioventricular block
  • 3) patients requiring pacing during surgery
  • 4) patients requiring postural change during surgery
  • 5) patients requiring coronary artery bypass grafting without oxygenator
  • 6) patients requiring artery clamp
  • 7) patients in a condition of cardiac tamponade
  • 8) patients with prior cardiopulmonary bypass surgery
  • 9) patients with prior blood vessel prosthesis implantation
  • 10) patients undergoing emergency operation
  • 11) Patients inappropriate for this study in the judgment of the investigator and/or subinvestigator

研究者

发起方
ihon Kohden Corporation

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