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NOT YET RECRUITING
NCT07608276
NA

Impact of NOL - Nociception Level Index Intraoperative Monitoring on Perioperative Outcomes in Spine Surgery - a Quality Improvement Pilot

Sponsor: Medasense Biometrics Ltd

View on ClinicalTrials.gov

Summary

The objective of this study is to evaluate the clinical impact of the NOL nociception level index monitoring on intraoperative and post operative patient outcomes and institutional metrics when used to guide intraoperative analgesia dosing in patients undergoing spine surgery under general anesthesia when compared to a case controlled retrospective cohort.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2026-05

Completion Date

2027-03

Last Updated

2026-05-27

Healthy Volunteers

No

Interventions

DEVICE

NOL guided intraoperative analgesia

The PMD-200 monitor with the NOL index will be used to guide analgesia dosing during anesthesia maintenance as an adjunct monitor used alongside other anesthesia monitors. If the NOL value is above 25 for sixty seconds or more, clinicians will evaluate whether more analgesia is needed. If the NOL value is below 25 the patient is considered to have adequately managed nociception.

Locations (1)

Thomas Jefferson University Hospital

Philadelphia, Pennsylvania, United States