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Clinical Trial Summary

The primary objective of this study is to verify, through a randomized, blinded, parallel clinical trial, the efficacy of bovine heparin from Eurofarma Laboratory product when compared to porcine heparin APP Pharmaceutical in patients undergoing surgery cardiovascular disease and who require cardiopulmonary bypass, through the control of hemostasis during and after surgery, based on measurements of markers of coagulation ACT, aPTT, anti-Xa heparin levels and the excessive blood loss (hemorrhage) after the end of surgery.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT01072955
Study type Interventional
Source L.A.L Clinica Pesquisa e Desenvolvimento Ltda.
Contact Alexandre Frederico, Dr.
Phone +551938293822
Email alexandre@lalclinica.com.br
Status Recruiting
Phase Phase 3
Start date April 2010
Completion date October 2011

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