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Cerebral Oximeter Comparison Study

NCT01655940 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2012-08-02

No results posted yet for this study

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

DEVICE

Somanetics cerebral oximeter

Somanetics cerebral oximeter

DEVICE

CASMED cerebral oximeter

CASMED cerebral oximeter

Sponsors & Collaborators

  • Nationwide Children's Hospital

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2011-10-31
Completion
2011-12-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01655940 on ClinicalTrials.gov