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Effect of Reduced Vasopressors on Mortality in ECMO-supported Cardiogenic Shock Patients

Recruitingn/aAges 18 Years - anyAllXiaotong Hou
NCT06862700 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this observational study is to learn about the association between vasopressor exposure levels and outcomes in adults with cardiogenic shock receiving VA-ECMO. The main question it aims to answer is: Does reduced exposure to vasopressors lower the 30-day mortality in patients with cardiogenic shock when receiving ECMO support? Participants who are receiving ECMO support for cardiogenic shock as part of their regular medical care will have their data collected, including information about their vasopressor use and mortality outcomes, over the course of the study.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adults (≥18 years) with cardiogenic shock requiring VA-ECMO support. * First-time ECMO initiation. * Venoarterial ECMO (VA-ECMO) as the initial mode. Exclusion Criteria: * Age \<18 years. * Severe pulmonary hypertension. * Vasopressor use for non-shock indications (e.g., bleeding, post-cardiopulmonary bypass vasoplegia). * Severe missing data.
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What it tests

  • Vasopressor Exposure Levels
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Where

1 site
Beijing Anzhen Hospital
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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