Clinical Trials Directory

Trials / Completed

CompletedNCT01408823

Pharmacokinetics of Aminocaproic Acid in Scoliosis Surgery

Pharmacokinetics of Epsilon-Aminocaproic Acid in Children and Adolescents With Scoliosis Undergoing Posterior Spinal Fusion

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
Children's Hospital of Philadelphia · Academic / Other
Sex
All
Age
8 Years – 18 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the pharmacokinetics of antifibrinolytic drug epsilon-aminocaproic acid (EACA) in children undergoing Posterior spinal fusion surgery (PSF) at The Children's Hospital of Philadelphia (CHOP) who receive EACA at the standard dose reported in the literature for this population and currently in use at CHOP.

Detailed description

Posterior spinal fusion surgery (PSF) can be associated with significant blood loss, and perioperative transfusion is common. Various strategies have been employed to decrease intraoperative blood loss and reduce transfusion in children undergoing PSF. The intraoperative administration of the antifibrinolytic drug epsilon-aminocaproic acid (EACA) is one such strategy that has been shown to be effective in this regard. This study will evaluate the pharmacokinetics of EACA in children undergoing PSF at CHOP who receive EACA at the standard dose reported in the literature for this population and currently in use at CHOP.

Conditions

Timeline

Start date
2011-07-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2011-08-03
Last updated
2013-08-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01408823. Inclusion in this directory is not an endorsement.