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临床试验/NCT06439732
NCT06439732已完成不适用

Impact of Using an Hemodynamic Monitoring System on Anesthetic Consumption During Abdominal Surgery

Fondazione Policlinico Universitario Agostino Gemelli IRCCS2 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2024年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
84
试验地点
2
主要终点
Reduction in Anesthetic consumption

研究概览

简要总结

In this study investigators will study the association between the use of an hemodynamic monitoring system and the anesthetic consumption in patients following major abdominal surgery. Investigators will randomise patients for a control group and an intervention group. Patients belonging to intervention group will be monitored with a non-invasively continue system (Acumen IQ cuff sensor), while the control group will be monitored with a non-invasive intermittent pressure system. The total amount of mL of Sevoflurane will be registered in both groups and the difference will be considered as the aim of our study

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • over 18 years of age
  • signature of informed medical consent

排除标准

  • NYHA III-IV
  • severe cardiac valvular diseases
  • absence of informed medical consent

结局指标

主要结局

Reduction in Anesthetic consumption

时间窗: During surgery

次要结局

  • number hypotensive episodes(during surgery)
  • duration hypotensive episodes(during surgery)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

RUSSO ANDREA

principal investigator

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

研究点 (2)

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