LiDCO Monitor Study

Completed · Not applicable

Conditions studied: Cardiac Surgery

In brief

This is a study to validate the utility and accuracy of the non-invasive device (LiDCOrapid monitor) during a period of phlebotomy and graded blood loss in patients who are having cardiac surgery.

Key facts

Study ID

NCT01567371

Run by

Nationwide Children's Hospital

People needed

30

Starts

2012-03-01

Expected to finish

2015-03-01

Last updated by the study team

2016-04-15

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients scheduled for intraoperative phlebotomy following anesthetic induction to obtain autologous blood for use following cardiopulmonary bypass and cardiac surgery.

Where it is running

• Nationwide Children's Hospital — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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