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临床试验/NCT07009730
NCT07009730已完成不适用

Clinical Outcomes Between Pulsatile and Non-Pulsatile Flow During Cardiopulmonary Bypass

Tribhuvan University Teaching Hospital, Institute Of Medicine.1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年7月23日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
ICU Length of Stay

研究概览

简要总结

The aim of this prospective, randomized study was to compare clinical outcomes of Pulsatile and non-pulsatile flow during Cardiopulmonary Bypass.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者

入选标准

  • patients undergoing Atrial Septal Defect closure and Mitral Valve replacement

排除标准

  • • Moderate and severe LVEF
  • • Patient with bleeding dysfunction;AKI ;deranged liver dysfunction\
  • • Patient/Surrogate decision maker not giving written informed consent

结局指标

主要结局

ICU Length of Stay

时间窗: 12 months

Measured in days from ICU admission to ICU discharge

次要结局

  • Duration of Cardiopulmonary Bypass (CPB)(12 months)

研究者

发起方
Tribhuvan University Teaching Hospital, Institute Of Medicine.
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ishwor Thapaliya

Principal Investigator

Tribhuvan University Teaching Hospital, Institute Of Medicine.

研究点 (1)

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