Clinical Trials Directory

Trials / Completed

CompletedNCT00604331

Effects of Pyruvate in Patients With Cardiogenic Shock and Intra-aortic Balloon Counterpulsation

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
8 (actual)
Sponsor
Herzzentrum Goettingen · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Pyruvate is an intermediate of energy metabolism and was shown to possess pronounced positive inotropic effects in vitro and in vivo without altering myocardial oxygen consumption. Moreover, it was shown that the effects of beta-adrenergic stimulation were potentiated. Thus, it might be possible to save catecholamines in patients with severe heart failure or cardiogenic shock. This study was designed to test the hemodynamic effects of pyruvate administered into a coronary artery in addition to intra-aortic balloon pump counterpulsation in patients with severe heart failure or in patients with acute myocardial infarction and cardiogenic shock after having performed percutaneous coronary intervention. A pronounced improvement in hemodynamics is expected to occur.

Conditions

Interventions

TypeNameDescription
DRUGPyruvatesodium pyruvate 300 mmol/L, 360 mL/h i.c. over 30 minutes.

Timeline

Start date
2008-08-01
Primary completion
2009-07-01
Completion
2009-07-01
First posted
2008-01-30
Last updated
2010-12-09

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00604331. Inclusion in this directory is not an endorsement.