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临床试验/DRKS00023189
DRKS00023189暂停不适用

Continuous and non-invasive determination of cardiac output: a triple comparison in clinical practice

Klinik und Poliklinik für Anästhesiologie, Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf0 个研究点目标入组 108 人开始时间: 2020年10月2日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
108

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Patients having-cardiac surgery with postoperative monitoring in the ICU who require invasive extended hemodynamic monitoring (transpulmonary thermodilution, pulmonary artery catheter) for clinical indications unrelated to the study
  • Adult patients (patients aged = 18 years)

排除标准

  • Patients with pronounced edema in the hands
  • Patients with vascular implants at the sites of non-invasive BP measurement (fin-gers and upper arms, respectively)
  • Patients with pronounced disturbance of peripheral blood circulation (peripheral artery disease of Fontaine state II and above, Raynaud syndrome, a-v-shunt etc.)
  • Patients with tonic seizures and/or excessive movements
  • Patients with history of arrhythmias
  • Patients with arteriosclerosis
  • Patients with atrial fibrillation
  • Patients with valvular disease of grade 2 or above
  • Patients with cardiac assist devices
  • Patients who, in addition to invasive BP monitoring, require NIBP measurements unrelated to the investigational devices
  • Patients who obtain vasoactive medications on the same arm as used for upper-arm NIBP measurements from the NiCCI System
  • Patients with a large lateral difference in BP (> 15 mmHg for systolic BP and/or >10 mmHg for diastolic BP) or with same arm measurement differences > 10mmHg in systolic or diastolic BP during assessment of lateral differences
  • Capillary refill-time > 2 seconds

研究者

发起方
Klinik und Poliklinik für Anästhesiologie, Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf

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