Cardiogenic Shock Working Group Registry
Launched by TUFTS MEDICAL CENTER · Dec 22, 2020
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
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
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
Similar Trials