The primary purpose of this study is to compare the analgesia nociception index-guided anesthesia and standard anesthesia on remifentanil requirement in desflurane anesthesia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
68
Maintaining the blood pressure based on analgesia nociception index of \>50 value
Maintaining the blood pressure based on anesthesiologist's decision
Remifentanil requirement
Assessing the total dose of remifentanil administered from skin incision until skin suture
Time frame: at time of the end of skin suture (up to 4 hours)
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