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Intraoperative M-Entropy Measurements

NCT00599066 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 24

Last updated 2017-04-14

No results posted yet for this study

Summary

The purpose of this study is to learn more about an Entropy monitor that the anesthesiologist will be using.

Conditions

  • General Anesthesia

Interventions

DEVICE

study cases

Application of a second M-Entropy probe on the forehead of the patient, which will happen in the OR along with the application of other monitors immediately before induction of general anesthesia.

Sponsors & Collaborators

  • University of Oklahoma

    lead OTHER

Principal Investigators

  • Mehemet Ozcan, MD · The University of Oklahoma Health Sciences Center, Department of Anesthesiology

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-06-30
Completion
2009-04-30

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 NCT00599066 on ClinicalTrials.gov