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
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