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RECRUITING
NCT06432894

Performance Evaluation of ANI in Patients Under General Anesthesia With Remimazolam

Sponsor: Catholic Kwandong University

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine whether Analgesia Nociception Index (ANI) can effectively reduce the dose of opioid in patients who underwent general anesthesia using remimazolam.

Official title: Performance Evaluation of Analgesia Nociception Index (ANI) in Patients Under General Anaesthesia With Remimazolam: a Prospective Observational Study

Key Details

Gender

All

Age Range

20 Years - 79 Years

Study Type

OBSERVATIONAL

Enrollment

30

Start Date

2024-04-23

Completion Date

2025-06-11

Last Updated

2024-05-30

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

Analgesia Nociception Index, remimazolam

The purpose of this study is to determine the validity of ANI in patients undergoing surgery with remifentanil and remimazolam. During this study, remimazolam infusion rate is determined by the pharmacopoeia. Remifentanil infusion rate is determined based on the patient's vital signs, systemic status and pain levels. And remifentanil is administrated via targeted infusion control using the Minto model. ANI scores, vital signs, remifentanil infusion rate are collected at predetermined time points according to the protocol from the start to the end of the surgery.

Locations (1)

Catholic-Kwandong University, School of Medicine

Incheon, South Korea