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RECRUITING
NCT06804434
NA

Impact of Intraoperative Non-invasive Analgesia Monitoring Using Nociception Level Index on Patient Management

Sponsor: Osoian Cristiana

View on ClinicalTrials.gov

Summary

This prospective randomised clinical trial aims to assess the impact of intraoperative nociception monitoring using NOL on anesthetic management during major abdominal surgery. Additionally, the study will objectively evaluate using NOL how intravenous lidocaine administration, influences opioid requirements and the effect of this multimodal approach on early postoperative outcomes. The investigators hypothesize that NOL-guided intraoperative opioid administration reduces both intraoperative and postoperative opioid use, positively influencing 24-hour outcomes. Furthermore, the addition of intraoperative lidocaine in NOL-guided analgesia may further decrease opioid consumption.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2023-05-18

Completion Date

2026-02-01

Last Updated

2025-02-03

Healthy Volunteers

No

Interventions

DRUG

Lidocaine Intravenous Infusion

intravenous lidocaine 10 mg/ml continuous infusion

DEVICE

NOL

Intraoperative Nociception Level index monitoring and guided analgesia

Locations (1)

Regional Gastroenterology and Hepatology Institute Octavian Fodor

Cluj-Napoca, Cluj, Romania