Early Intra-aortic Balloon Pump Use After Venoarterial Extracorporeal Membrane Oxygenation
Condition(s) studied
Investigational drug(s) / intervention(s)
Early IABP use: Patients receive IABP for left ventricular unloading within 6 hours after VA-ECMO initiation.
Conventional approach: Patients do not receive mechanical unloading within 6 hours after VA-ECMO initiation.
Study summary
The goal of this multicenter, randomized trial is to compare early early left ventricular unloading by Intra-aortic Balloon Pump (IABP) versus conventional approach in patients with cardiogenic shock (CS) undergoing venoarterial extracorporeal membrane oxygenation (VA-ECMO). The main question it aims to answer is :
• If left ventricular unloading by IABP as compared with the conventional approach will improve the outcomes in patients undergoing VA-ECMO.
Eligibility
Primary outcome measure(s)
- 30-day mortality — 30 days
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Beijing Anzhen Hospital | Beijing | Beijing Municipality | Recruiting |
More Beijing Anzhen Hospital trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06872021 on ClinicalTrials.gov ↗ ← All trials in China