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COMPLETED
NCT05615441
NA

Effect of Nociception Level Monitoring During Remimazolam-based Total Intravenous Anesthesia on Intraoperative Opioid Requirements and Postoperative Pain

Sponsor: Yonsei University

View on ClinicalTrials.gov

Summary

This study aims to investigate whether the use of nociception monitoring during general anesthesia with remimazolam-based total intravenous anesthesia has an effect on intraoperative opioid requirements and postoperative pain. This study is a randomized trial with a 50% probability of being assigned to either group. Randomization will be done by an anesthesiologist not involved in anesthesia or postoperative outcome assessment. Patients and the investigator in charge of postoperative outcomes assessment will be blinded to group allocation.

Key Details

Gender

All

Age Range

19 Years - 64 Years

Study Type

INTERVENTIONAL

Enrollment

54

Start Date

2023-07-17

Completion Date

2025-11-21

Last Updated

2026-06-23

Healthy Volunteers

No

Interventions

DEVICE

Analgesia Nociception Index monitor

Patients will receive remimazolam-based total intravenous general anesthesia with nociception monitoring with the ANI monitor

DEVICE

Standard monitoring

Patients will receive remimazolam-based total intravenous general anesthesia based on hemodynamic monitoring and without nociception monitoring

Locations (1)

Yonsei University Health System, Severance Hospital

Seoul, South Korea