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Clinical Trial Summary

The investigators hypothesized that intraoperative opioid consumption would be different between remimazolam and propofol if the ANI-guided remifentanil continuous infusion rate was adjusted when the depth of anesthesia was maintained at similar depths with remimazolam or propofol under total intravenous anesthesia. The purpose of this study is to compare the intraoperative remifentanil requirement in patients undergoing total knee arthroplasty when the intraoperative remifentanil dose adjustment was performed under the ANI guidance while maintaining a similar depth of anesthesia with remimazolam or propofol.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05322902
Study type Interventional
Source Gangnam Severance Hospital
Contact
Status Completed
Phase N/A
Start date June 2, 2022
Completion date July 18, 2023

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