HemoSonics-UVA HemoSonics-UVA Cardiac Surgery Clinical Study Protocol

Completed

Conditions studied: Coronary Artery Disease

In brief

This study compares the results of current standard coagulation measurement devices to the Quantra System, a new device, using small amount of extra blood obtained during routine blood draws in cardiac surgery patients.

Key facts

Study ID

NCT02456467

Run by

University of Virginia

People needed

50

Starts

2015-04-01

Expected to finish

2015-08-01

Last updated by the study team

2016-10-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subject is scheduled for cardiac surgery involving bypass circuit
• Subject is older than 18 years
• Subject is willing to participate and he/she has signed a consent form

You may not qualify if…

• Subject is unable to provide written informed consent
• Subject is incarcerated at the time of the study
• Subject is affected by any condition that, in the opinion of the surgical team, may pose additional risks
• Patients with renal disease (defined as serum creatinine greater than 1.5 mg/dl)
• Patients with history of active liver disease
• Patients on emergency cases
• Patients on heparin anticoagulation before the beginning of the study

Where it is running

• University of Virginia Health System — Charlottesville, Virginia, United States

Full record on ClinicalTrials.gov

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