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Early Intra-aortic Balloon Pump Use After Venoarterial Extracorporeal Membrane Oxygenation

NCT06872021 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 358

Last updated 2026-03-24

No results posted yet for this 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.

Conditions

  • ECMO

Interventions

OTHER

Early IABP use

Patients receive IABP for left ventricular unloading within 6 hours after VA-ECMO initiation.

OTHER

Conventional approach

Patients do not receive mechanical unloading within 6 hours after VA-ECMO initiation.

Sponsors & Collaborators

  • Beijing Anzhen Hospital

    lead OTHER

Principal Investigators

  • Xiaotong Hou, MD, PhD · Beijing Anzhen Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-22
Primary Completion
2028-09-01
Completion
2028-12-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06872021 on ClinicalTrials.gov