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Aortic Balloon Counterpulastion in Myocardial Infarction Related Shock

Intra-Aortic Balloon Counterpulsation in Patients With Acute Myocardial Infarction Complicated by Cardiogenic Shock - The Prospective, Randomised IABP SHOCK Trial for Attenuation of Multi-Organ Dysfunction Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00469248
Acronym
IABPSHOCK
Enrollment
45
Registered
2007-05-04
Start date
2003-03-31
Completion date
2004-06-30
Last updated
2007-05-04

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

Conditions

Cardiogenic Shock, Myocardial Infarction

Keywords

Myocardial infarction, Cardiogenic shock, Systemic inflammatory response syndrome, Percutaneous coronary intervention, aortic balloon counterpulsation

Brief summary

The role of intra aortic balloon counterpulsation in patients experiencing acute myocardial infarction with shock is not established. We hypothesised that use of such a device would lead to improved outcomes in these patients.

Detailed description

Patients undergoing percutaneous coronary intervention (PCI) for acute myocardial infarction (AMI) with cardiogenic shock (CS) are often treated with Intra-aortic balloon pump counterpulsation (IABP) although the evidence to support this is limited. We conducted a prospective, randomised clinical trial, of IABP as an addition to PCI centred therapy, in patients with AMI complicated by CS. 45 patients with AMI and CS undergoing PCI were randomised to care with or without IABP. Over 4 days, APACHE II scores, haemodynamic parameters, inflammatory markers and BNP levels were collected to assess the impact of IABP treatment on CS triggered multi organ dysfunction syndrome (MODS).

Interventions

DEVICEIntra-aortic balloon pump counterpulsation

Sponsors

Martin-Luther-Universität Halle-Wittenberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Acute myocardial infarction * Cardiogenic shock

Exclusion criteria

* Absent peripheral pulses * Mechanical complications of myocardial infarction

Design outcomes

Primary

MeasureTime frame
APACHE II SCORE4 days

Secondary

MeasureTime frame
Haemodynamic state4 days
BNP levels4 days
Inflammatory activation4 days
Mortality4 days

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 1, 2026