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临床试验/NCT04682483
NCT04682483招募中不适用

Cardiogenic Shock Working Group Registry

Tufts Medical Center16 个研究点 分布在 1 个国家目标入组 5,000 人开始时间: 2017年12月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
5,000
试验地点
16
主要终点
Rate of Mortality

研究概览

简要总结

The Cardiogenic Shock Working Group is a multicenter registry where we collect de-identified clinical variables from the medical records and follow-up phone calls of shock patients from multiple institutions and centralize this data to a single registry for analysis of clinical outcomes.

详细描述

The Cardiogenic Shock Working Group is an Academic Research Consortium involving multiple medical centers within the United States and includes a multicenter registry for patients with cardiogenic shock. De-identified clinical variables are collected from medical records and follow-up phone calls. There is currently no central database for cardiogenic shock, therefore analysis of cardiogenic shock on a larger scale is limited. A goal of the Cardiogenic Shock Working Group is to create a centralized registry, compiled of data from multiple institutions, to analyze clinical outcomes. The Cardiogenic Shock Working Group Registry will include a retrospective arm, where data is collected during the course of the hospital stay, and a prospective arm, where long-term outcomes will be assessed.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

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

  • Patients must have cardiogenic shock.
  • Cardiogenic shock is defined by at least one of the two categories below:
  • At least 2 of the following concurrently at any point during the index hospitalization:
  • Cardiac Index < 2.2
  • PAPI < 1.0
  • Cardiac Power Output ≤ 0.6
  • MAP < 60mmHg or a >30mmHg drop in MAP from baseline
  • SBP < 90mmHg or a >30mmHg drop in SBP from baseline
  • Pulse > 100
  • Require at least one acute mechanical circulatory support device, vasopressor or inotrope to maintain values above the above target.
  • Post-cardiotomy patients must meet the inclusion criteria 72 hours after their surgery to be included in this registry.

排除标准

  • 未提供

研究组 & 干预措施

Cardiogenic Shock Patients

Cardiogenic Shock patients eligible for this study are defined by at least one of the two categories below.

  1. Patients have at least 2 of the following concurrently at any point during the index hospitalization: MAP < 60mmHg or a >30mmHg drop in MAP from baseline, SBP < 90mmHg or a >30mmHg drop in SBP from baseline, Pulse > 100, Cardiac Index < 2.2, Cardiac Power Output ≤ 0.6 or PAPI < 1.0.
  2. Patients require the use of at least 1 vasopressor, inotrope or acute mechanical circulatory support device to maintain values above the above targets.

干预措施: Vasopressor (Drug)

Cardiogenic Shock Patients

Cardiogenic Shock patients eligible for this study are defined by at least one of the two categories below.

  1. Patients have at least 2 of the following concurrently at any point during the index hospitalization: MAP < 60mmHg or a >30mmHg drop in MAP from baseline, SBP < 90mmHg or a >30mmHg drop in SBP from baseline, Pulse > 100, Cardiac Index < 2.2, Cardiac Power Output ≤ 0.6 or PAPI < 1.0.
  2. Patients require the use of at least 1 vasopressor, inotrope or acute mechanical circulatory support device to maintain values above the above targets.

干预措施: Inotrope (Drug)

Cardiogenic Shock Patients

Cardiogenic Shock patients eligible for this study are defined by at least one of the two categories below.

  1. Patients have at least 2 of the following concurrently at any point during the index hospitalization: MAP < 60mmHg or a >30mmHg drop in MAP from baseline, SBP < 90mmHg or a >30mmHg drop in SBP from baseline, Pulse > 100, Cardiac Index < 2.2, Cardiac Power Output ≤ 0.6 or PAPI < 1.0.
  2. Patients require the use of at least 1 vasopressor, inotrope or acute mechanical circulatory support device to maintain values above the above targets.

干预措施: Acute Mechanical Circulatory Support Devices (Device)

结局指标

主要结局

Rate of Mortality

时间窗: 1 year after discharge

Death in subjects during the time frame.

次要结局

  • Rate of Re-hospitalization(1 year after discharge)
  • New York Heart Association (NYHA) Class(1 year after discharge)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (16)

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