LiDCO Monitor Study

Nationwide Children's Hospital

Status: Completed

Conditions: Cardiac Surgery

Treatments: Device: LiDCO rapid monitor

Study type: Interventional

Funder types: Other

Identifiers

NCT01567371

IRB12-00096

Details and patient eligibility

About

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.

Enrollment: 30 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

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

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

LiDCO rapid monitor

Experimental group

Treatment:

Device: LiDCO rapid monitor