NCT01655940

Cerebral Oximeter Comparison Study

Comparison of the FORE-SITE and INVOS Cerebral Oximeters During Cardiac Surgery

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 50 (actual)
• Sponsor: Nationwide Children's Hospital · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

In this prospective study to try to standardize the care for patients, the investigators are planning to compare two cerebral oximeters currently in use at NCH in terms of their accuracy in determining the cerebral oxygen saturation as determined by jugular bulb oxygen saturation. Also, the investigators will compare these devices in terms of their response to changes in hemodynamics that occur during cardiac surgery.

Conditions

• Cardiac Bypass Patients

Interventions

Type	Name	Description
DEVICE	Somanetics cerebral oximeter	Somanetics cerebral oximeter
DEVICE	CASMED cerebral oximeter	CASMED cerebral oximeter

Timeline

• Start date: 2011-05-01
• Primary completion: 2011-10-01
• Completion: 2011-12-01
• First posted: 2012-08-02
• Last updated: 2012-08-02

Locations

1 site across 1 country: United States