Measurement of nociception and prediction of movement during combined general epidural anesthesia in ASA I-III patients undergoing major abdominal surgery using bilateral frontal EEG measurements and hemodynamic parameters .

eiden University Medical Center, dept of Anesthesiology0 sites60 target enrollmentTBD

ConditionsIn the current study we will measure CVI as a measure of adequate analgesia in ASA 1-3 patients during elective abdominal surgery under fentanyl/sevoflurane/epidural anesthesia. We will monitor patient movement as primary correlate to CVI and cardiovascular parameters as secondary correlates (eg, cardiac output, pulse transit time, blood pressure and heart rate).

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: In the current study we will measure CVI as a measure of adequate analgesia in ASA 1-3 patients during elective abdominal surgery under fentanyl/sevoflurane/epidural anesthesia. We will monitor patient movement as primary correlate to CVI and cardiovascular parameters as secondary correlates (eg, cardiac output, pulse transit time, blood pressure and heart rate).
Sponsor: eiden University Medical Center, dept of Anesthesiology
Enrollment: 60
Status: Recruiting
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

2 years ago

Study Type

Interventional

Investigators

Sponsor

eiden University Medical Center, dept of Anesthesiology

Eligibility Criteria

Inclusion Criteria

•1\. Age: 18\-80 years;
•2\. Sex: Male or female;

Exclusion Criteria

•1\. Age: \< 18 or \> 80 years;
•2\. Unable to give written informed consent;

Outcomes

Primary Outcomes

Not specified

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