Back to Trials
NCT04682483Recruiting

Cardiogenic Shock Working Group Registry

Tufts Medical Center

Start Date

12/4/2017

Completion Date

6/1/2026

Summary

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.

Detailed Description

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.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Patients must have cardiogenic shock. Cardiogenic shock is defined by at least one of the two categories below: 1. 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 2. 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.

Interventions

DRUG

Vasopressor

DRUG

Inotrope

DEVICE

Acute Mechanical Circulatory Support Devices

Interested in This Trial?

Contact the trial locations directly using the information below to learn more about enrollment.

Expressing interest lets you review the study and consent before we connect you with the research site.

Conditions

Cardiogenic Shock

Locations

Cleveland Clinic Florida

Weston, Florida 33331

United States

Northwestern Medicine

Chicago, Illinois 60611

United States

University of Chicago

Chicago, Illinois 60612

United States

Maine Medical Center

Portland, Maine 04102

United States

Tufts Medical Center

Boston, Massachusetts 02111

United States

Beth Israel Deaconess Medical Center

Boston, Massachusetts 02215

United States

Hackensack Meridian Health

Hackensack, New Jersey 07601

United States

Columbia University Irving Medical Center

New York, New York 10032

United States

Providence St. Vincent Heart Clinic

Portland, Oregon 97225

United States

Allegheny General Hospital

Pittsburgh, Pennsylvania 15212

United States

University Of Pittsburgh Medical Center

Pittsburgh, Pennsylvania 15261

United States

Baylor Scott & White Advanced Heart Failure Clinic

Dallas, Texas 75201

United States

University of Texas Medical Branch

Galveston, Texas 77555

United States

Houston Methodist Hospital

Houston, Texas 77030

United States

Inova Health System

Falls Church, Virginia 22042

United States

University of Washington Medical Center

Seattle, Washington 98195-9472

United States