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Cardiogenic Shock Working Group Registry

Launched by TUFTS MEDICAL CENTER · Dec 22, 2020

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Cardiogenic Shock Mechanical Circulatory Support Hemodynamics Heart Failure Acute Myocardial Infarction Registry Critical Care Clinical Outcomes Research

ClinConnect Summary

The Cardiogenic Shock Working Group Registry is a clinical trial that aims to gather and analyze information about patients experiencing cardiogenic shock, a serious condition where the heart cannot pump enough blood to meet the body's needs. Researchers will collect data from patients’ medical records and follow-up phone calls from multiple hospitals to better understand the outcomes of this condition and improve future treatments.

To be eligible for this study, participants must be diagnosed with cardiogenic shock, which can be identified by specific medical signs or the need for special devices to help support their heart function. The trial is open to all patients aged 65 and older. If you or a loved one is interested in participating, you can expect to have your health information reviewed and followed up on, but your personal details will remain confidential. This registry is important because it will help researchers learn more about cardiogenic shock and potentially improve care for future patients.

Gender

ALL

Eligibility criteria

  • 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.

About Tufts Medical Center

Tufts Medical Center is a leading academic medical institution located in Boston, Massachusetts, renowned for its commitment to advancing healthcare through innovative research and clinical trials. As a sponsor of clinical trials, Tufts Medical Center leverages its expertise in diverse medical disciplines to develop and test new therapies, enhance patient care, and contribute to the scientific community. With a focus on collaboration and rigorous methodologies, the center aims to translate research findings into practical applications that improve health outcomes for patients locally and globally. Its dedication to excellence is reflected in its partnerships with academic institutions, industry leaders, and healthcare organizations.

Locations

Chicago, Illinois, United States

Boston, Massachusetts, United States

Portland, Maine, United States

Pittsburgh, Pennsylvania, United States

Houston, Texas, United States

Boston, Massachusetts, United States

Galveston, Texas, United States

Weston, Florida, United States

Pittsburgh, Pennsylvania, United States

Falls Church, Virginia, United States

New York, New York, United States

Chicago, Illinois, United States

Chicago, Illinois, United States

Hackensack, New Jersey, United States

Portland, Oregon, United States

Dallas, Texas, United States

Seattle, Washington, United States

Patients applied

0 patients applied

Trial Officials

Reshad Garan, MD

Study Director

Beth Israel Deaconess Medical Center

Claudius Mahr, DO

Study Director

University of Washington

Jaime Hernandez-Montfort, MD

Study Director

Cleveland Clinic Foundation-Florida

Daniel Burkhoff, MD PhD

Study Director

CardioVascular Research Foundation

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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