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Clinical Trial Summary

The investigators conduct a random assignment into either the remimazolam group or the propofol group. Depending on the group assignment, either remimazolam (0.2 mg/kg) or propofol (1.0 mg/kg) is administered. If necessary, additional doses of remimazolam (0.1 mg/kg) or propofol (0.5 mg/kg) are given. The standard anesthesia procedure of our institution is followed, and blood pressure data recorded during the surgery is analyzed (mean arterial pressure <65mmHg is defined as hypotension).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06093971
Study type Interventional
Source Yonsei University
Contact So Yeon Kim
Phone 82-2-2228-2429
Email KIMSY326@yuhs.ac
Status Not yet recruiting
Phase N/A
Start date November 2023
Completion date September 2025

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