Clinical Trials Directory

Trials / Terminated

TerminatedNCT01965730

Dosing of Amicar and Measure of Fibrinolysis by TEG During Cardiac Surgery

The Effect of Standard vs Aggressive Dosing Regimens for Epsilon-aminocaproic Acid on a Quantifiable Parameter of Fibrinolysis as Measured by Thromboelastography

Status
Terminated
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
8 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

This study hopes to determine the optimal antifibrinolytic dosing to decrease bleeding and blood transfusion after cardiac surgery without increasing adverse events

Conditions

Interventions

TypeNameDescription
DRUGepsilon-aminocaproic acid (EACA)

Timeline

Start date
2013-01-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2013-10-18
Last updated
2019-05-02

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01965730. Inclusion in this directory is not an endorsement.

Dosing of Amicar and Measure of Fibrinolysis by TEG During Cardiac Surgery (NCT01965730) · Clinical Trials Directory