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A prospective randomized controlled trial of VA-ECMO combined with intra-aortic balloon pump for acute myocardial infarction-induced cardiogenic shock.

A prospective randomized controlled trial of VA-ECMO combined with intra-aortic balloon pump for acute myocardial infarction-induced cardiogenic shock.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115392
Enrollment
Unknown
Registered
2025-12-25
Start date
2026-01-01
Completion date
Unknown
Last updated
2026-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cardiogenic shock caused by acute myocardial infarction

Interventions

VA-ECMO plus IABP group:Combined with intra-aortic balloon pump therapy
VA-ECMO alone group:Receiving VA-ECMO therapy

Sponsors

The People's Hospital Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria include adult patients (age >= 18 years) diagnosed with cardiogenic shock following acute myocardial infarction, receiving veno-arterial extracorporeal membrane oxygenation (VA-ECMO), with or without IABP use.

Exclusion criteria

Exclusion criteria: Patients with a history of stroke, prior percutaneous coronary intervention, or coronary artery bypass grafting were excluded from the study.

Design outcomes

Primary

MeasureTime frame
In-hospital all-cause mortality;

Secondary

MeasureTime frame
Other: All-cause mortality, VA-ECMO weaning success rate, gastrointestinal bleeding, limb ischemia, pump thrombosis, duration of mechanical ventilation, ECMO duration, ICU length of stay, hospital length of stay, transfusion of frozen plasma, transfusion of red blood cells, and incidence of other complications.;

Countries

China

Contacts

Public ContactHuang Jingbin

The People’s Hospital of Guangxi Zhuang Autonomous Region

hjb010222@163.com+86 139 7875 3833

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026