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临床试验/NCT04369573
NCT04369573终止4 期

Early Intra-aortic Balloon Pump Placement in Acute Decompensated Heart Failure Complicated by Cardiogenic Shock: a Randomized Clinical Trial

Niguarda Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年5月4日最近更新:
适应症

试验速览

阶段
4 期
状态
终止
入组人数
100
试验地点
2
主要终点
Survival

研究概览

简要总结

The aim of the study is to demonstrate the superiority of early intra-aortic balloon pump implantation at admission over local clinical practice (pharmacological only) in acute decompensated heart failure patients with cardiogenic shock, with respect to 60-day survival or successful bridge to heart replacement therapies (heart transplant or Left Ventricular Assist Device implantation).

详细描述

Cardiogenic shock (CS) is the most severe form of acute heart failure, with in-hospital mortality up to 50%. Failure to improve mortality has been reported, despite observed improvements in hemodynamics. Previous studies on CS have almost exclusively been focused on CS following an acute coronary syndrome (ACS). Chronic heart failure patients with acute decompensation (ADHF) and CS represent a unique physiologic phenotype compared with ACS patients, which may lead to a differential response to device therapy. Recent evidences emphasize that intra-aortic balloon pump (IABP) is not recommended for patients with ACS-related CS, but it is associated with a high likelihood of bridge to durable Left Ventricular Assist Device or heart transplant without the need for escalation to more potent temporary mechanical circulatory support devices, when implanted in ADHF patients. Data retrieved from the available literature in the setting of patients with CS not related to ACS are poor even in large, well-reported registries.

Accordingly, Altshock-2 trial has been designed to test the superiority of early IABP implantation at admission over local clinical practice (pharmacological only) in ADHF patients with CS, with respect to 60-day survival or successful bridge to heart replacement therapies

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
None

盲法说明

Open

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Survival

时间窗: 60 days

Rate

Successful bridge to heart replacement therapies, namely heart transplantation or left ventricular assist device implantation

时间窗: 60 days

Number of participants to heart transplant or Left Ventricular Assist Device implantation

次要结局

  • Maximum duration of inotropic/vasopressor therapy among the two groups(Through study completion, an avererage of 30 days)
  • Maximum inotropic score among the two groups(Through study completion, an avererage of 30 days)
  • Maximum sequential organ failure assessment (SOFA)(Through study completion, an avererage of 30 days)
  • early IABP vs standard(60 days)
  • Renal replacement therapy, namely any need of replacement of kidney function due to renal failure by means of the following techniques: continuous hemofiltration and hemodialysis, intermittent hemodialysis, and peritoneal dialysis(60 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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