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OpenTrials
Completed

NCT Number: NCT00697723

Arterial Versus Venous Graft Recruitment by Intra-Aortic Balloon Pump

The aim of this study is to evaluate the different performance of arterial and venous graft with intra-aortic balloon pump support following coronary artery bypass.

Completed

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of Magna Graecia - Cardiac Surgery unit

Catanzaro, 88100, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All patients undergoing coronary artery bypass surgery

Exclusion criteria

  • Aortic insufficiency;
  • Diffuse atherosclerosis impeding intra-aortic balloon pump introduction

Treatment and study plan

Transit-time flowmetry

Procedure

Transit-time flowmetry during 1:1 IABP assistance and when IABP is turned off

Primary outcomes

  1. Hospital mortality and morbidity

    Time frame: three years

Secondary outcomes

  1. Transit-time flowmetry

    Time frame: three years

Sponsors and collaborators

Lead sponsor

University Magna Graecia

Other

Registry information

Important dates

Study start
2005
Primary completion
2008
Study completion
2008
First posted
Jun 16, 2008
Registry last updated
Jun 16, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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