NL-OMON33353
Completed
Not Applicable
Measurement of nociception and prediction of movement during combined general (sevoflurane/fentanyl)-epidural anesthesia in ASA I-III patients undergoing major abdominal surgery using bilateral frontal EEG measurements and hemodynamic parameters (pulse transit time, cardiac output, blood pressure and heart rate) - CVI
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- periopertieve pijn
- Sponsor
- eids Universitair Medisch Centrum
- Enrollment
- 90
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Age: 18\-80 years;
- •Sex: male or female;
- •Surgery: elective abdominal surgery lasting at least 2 hours. This includes gynecological procedures (eg., abdominal hysterectomies), urological procedures (eg., radical prostatectomies), GI\-surgery (eg., colon surgery);
- •ASA status: 1, 2 or 3\.
Exclusion Criteria
- •Age: \< 18 or \> 80 years;
- •Unable to give written informed consent;
- •Pregnancy/lactation;
- •Extreme obesity: BMI \> 35;
- •Perceived difficult intubation requiring muscle relaxation.
Outcomes
Primary Outcomes
Not specified
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