Measurement of nociceptive index during general anesthesia in ASA 1-3 patients undergoing elective surgery using the Nociception Level (NoL) index

Recruiting

• Conditions: patienten die een elective chirurgische ingreep ondergaan onder algehele anesthesie; Nociception; Pain

• Registration Number: NL-OMON38899
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 96

Inclusion Criteria

Patients undergoing elective surgery under general anesthesia

Exclusion Criteria

Age: < 18 or > 80 years;
Unable to give written informed consent;
Pregnancy/lactation;
Extreme obesity: BMI > 35;
Perceived difficult intubation.
Patients requiring a rapid sequence induction
Patients on beta-blockers

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>NoL</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Cardiovascular parameters incl. HR, BP and CO</p><br>