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Clinical Trial Summary

The ECMO-RESCUE study is a prospective, multicenter, non-randomized, cohort study. In this study, we aimed to assessed whether VA-ECMO treatment can improve the 30-day survival rate of patients with sepsis-induced refractory cardiogenic shock.


Clinical Trial Description

All patients who meet inclusion criteria and have no exclusion criteria are considered to be enrolled. During the period of study, the participants can decide whether to accept ECMO based on their personal conditions. If a patient is willing to accept ECMO treatment, we initiate VA-ECMO within 2 hours. Participants taking VA-ECMO during the period of study are referred to as cohort 1, and patients receiving only conventional therapy without ECMO belong to cohort 2. 30-day survival will be accessed to evaluate the survival benefit from ECMO therapy for sepsis-induced refractory cardiogenic shock. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05184296
Study type Interventional
Source Second Affiliated Hospital of Guangzhou Medical University
Contact Wei-yan Chen
Phone +8613751845652
Email [email protected]
Status Not yet recruiting
Phase N/A
Start date January 1, 2022
Completion date May 31, 2025

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