Cerebral Oximetric Monitoring of the Posterior Circulation

CompletedOBSERVATIONAL
Enrollment

13

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

April 30, 2008

Study Completion Date

April 30, 2008

Conditions
Congenital Heart Disease
Interventions
DEVICE

Cerebral oximeter sensor

The INVOS Cerebral Oximeter utilizes two electrodes to monitor cerebral oxygenation. The recommended placement of these electrodes is on the forehead to monitor the frontal cortex. In this study, one electrode will be placed in the normal position on the forehead, and the other will be placed at the base of the skull. The stickers will be placed on the patient at the beginning of surgery and removed at the end. The maximum amount of time that they will be on the patient's skin is approximately six hours. Application of the stickers and the data they provide will not alter the provider's treatment plan. This procedure will be used for all enrolled patients, whether they are enrolled in Part I or Part II.

Trial Locations (1)

55404

Children's Hospitals and Clinics of Minnesota, Minneapolis

All Listed Sponsors
lead

Children's Hospitals and Clinics of Minnesota

OTHER

NCT00751712 - Cerebral Oximetric Monitoring of the Posterior Circulation | Biotech Hunter | Biotech Hunter