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Use of Intra-aortic Balloon Pump Before Surgery for Acute Myocardial Infarction

A

Ataturk University

Status

Completed

Conditions

Coronary Bypass Graft Stenosis of Autologous Vessel
Coronary Artery Disease
Troponin
IABP - Disorder of Intra-Aortic Balloon Pump
Acute Myocardial Infarction

Treatments

Device: Intra-aortic Balloon Pump

Study type

Interventional

Funder types

Other

Identifiers

NCT06468982
AÜ-CVS-UA-01

Details and patient eligibility

About

The optimal timing of surgery in patients with acute myocardial infarction (AMI) and the utilization of preoperative intra-aortic balloon pumps (IABP) in these patients are subjects of ongoing discussion and disagreement. This study aimed to investigate the effects of preoperative IABP on troponin levels, surgical timing, and intraoperative and postoperative outcomes for patients with AMI who undergo coronary artery bypass grafting (CABG).

Full description

Percutaneous coronary intervention (PCI) is the first treatment for myocardial ischemia; however, if left main coronary artery disease, multivessel disease, or complex architecture disable PCI, 10% of patients may need coronary artery bypass grafting (CABG). Abstinence from surgical reperfusion in patients with acute myocardial infarction (AMI) may be justified due to surgery's 50% mortality rate. An intra-aortic balloon pump (IABP) can help patients who have ongoing ischemia and high cardiac enzymes because it changes the way the heart uses oxygen by increasing coronary blood flow and lowering afterload. Some guidelines do not recommend the use of IABP in patients with AMI except for mechanical complications or shock. Nevertheless, it is commonly acknowledged that the specific criteria for employing IABP differ among clinics and are determined by clinical expertise. Patients with AMI who have impaired coronary perfusion and require surgical revascularization can benefit from preoperative intra-aortic balloon pump (IABP) support. This intervention leads to reorganization of coronary perfusion, resulting in a decrease in elevated troponin levels and quicker myocardial recovery.

Enrollment

156 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who have had acute myocardial infarction and have been decided on coronary surgical revascularization

Exclusion criteria

  • mechanical complications of Acute Myocardial Infarction (such as a ruptured chordal or ventricular septum)
  • peripheral arterial disease
  • renal failure
  • history of cerebrovascular accident
  • acute cardiogenic shock and cardiac arrest
  • reoperation and combined operations

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

156 participants in 2 patient groups

Group A (IABP support)
Active Comparator group
Description:
Patients who are receiving intra-aortic balloon pump support during the preoperative period
Treatment:
Device: Intra-aortic Balloon Pump
Group B (control group; without IABP support)
No Intervention group
Description:
Patients who did not receive intra-aortic balloon pump support in the preoperative period; control group

Trial documents
2

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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