Investigating treatment outcomes for patients with cardiogenic shock
Official title: SafeTy and Outcome of contemPorary Treatment Strategies for Cardiogenic SHOCK - an International, Observational Registry
Run by Universitätsklinikum Hamburg-Eppendorf · NCT03313687 · Data updated 2026-11-12
This study looks at how different treatments for cardiogenic shock work for patients to see which ones are most effective and what side effects they might have.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2500 (estimated) |
| Sponsor | Universitätsklinikum Hamburg-Eppendorf Academic / other |
| Locations | 1 site (Hamburg) |
| Status | Recruiting |
| Started | September 1, 2017 |
| Main results expected | December 31, 2030 |
| Study ends | December 31, 2031 |
| Registry record updated | October 7, 2021 |
| Trial ID | NCT03313687 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with cardiogenic shock who are being treated at a tertiary care hospital.
✕Probably not a fit
Patients under the age of 17 will not benefit from this study as they are excluded from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This international observational registry aims to assess the clinical outcomes of patients experiencing cardiogenic shock. The study focuses on various treatment strategies, including interventional therapies and mechanical circulatory support, while monitoring the drug therapies and devices used in these patients. By documenting the practices at participating sites, the study seeks to provide insights into the effectiveness and side effects of current treatment approaches for cardiogenic shock.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies and outcomes for patients suffering from cardiogenic shock.
How similar studies have gone: Other studies focusing on treatment outcomes in cardiogenic shock have shown promise, indicating that this approach is relevant and potentially beneficial.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients with cardiogenic shock treated at a tertiary care hospital. Exclusion Criteria: * Age ≤17 years.
Where it's running
-
University Heart Center
Hamburg, Germany Recruiting
Study contacts
- Principal investigator: Dirk Westermann, MD — Uhz
- Study coordinator: Benedikt Schrage, MD
- Email: b.schrage@uke.de
- Phone: +49 40 7410 18135
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Evaluating a noninvasive tissue sensor to detect cardiogenic shock earlier in heart patients
This pilot, noninvasive study tests whether the NIRSense wearable can help detect deterioration in adults with cardiogenic shock risk due to heart attack or heart failure.
-
Safety and Efficacy of an Extracorporeal Ventricular Assist System for Cardiogenic Shock
This study tests whether an extracorporeal ventricular assist device can safely provide short-term heart support and help patients with cardiogenic shock or trouble weaning from bypass.
-
Left Ventricular Support and Advanced Monitoring in AMI–Cardiogenic Shock: Immediate Impella Use and PAC/Monitoring vs Standard Care
In adults with heart attack-related cardiogenic shock, this trial tests whether using an Impella left ventricular assist device and/or protocolized pulmonary artery catheter monitoring improves survival compared with standard care.
-
CRP Apheresis for infarct-related cardiogenic shock
This study tests whether selectively removing C-reactive protein with apheresis, in addition to standard care, helps people with cardiogenic shock after a heart attack.
-
Compare two ventilator modes in adults with cardiac ICU needs and invasive ventilation
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.