Effect of Nociception Level Monitoring During Remimazolam-based Total Intravenous Anesthesia on Intraoperative Opioid Requirements and Postoperative Pain
NCT05615441 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58
Last updated 2022-11-14
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.
Conditions
- Adult Patients Aged 19-64, Scheduled for Elective Arthroscopic Knee Surgery
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
Sponsors & Collaborators
-
Yonsei University
lead OTHER
Principal Investigators
-
Seokyung Shin · Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 19 Years
- Max Age
- 64 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-02
- Primary Completion
- 2024-11-01
- Completion
- 2024-11-01
Countries
- South Korea
Study Locations
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