Comparing postoperative analgesics requirements and complications between conventional and model-based infusion strategy of intravenous patient-controlled analgesia in patients who undergoing robot assisted laparoscopic radical prostatectomy Group A: conventional intravenous patient-controlled analgesia, Group B: model-based infusion strategy of intravenous patient-controlled analgesia
The investigators compared postoperative analgesics requirements and complications between conventional and model-based infusion strategy of intravenous patient-controlled analgesia (IV PCA) in patients who undergoing robot assisted laparoscopic radical prostatectomy (RALP) Group A: conventional IV PCA, Group B: model based IV PCA 1. Primary endpoint: comparison of postoperative analgesic requirements in patient undergoing robot assisted laparoscopic radical prostatectomy (RALP) between conventional patient controlled analgesia (PCA) (Group A) and effective-compartment based dosing strategy of PCA (Group B) 2. Secondary endpoint: 1) VAS analysis between two groups, 2) postoperative nausea and vomiting analysis between two groups, 3) complication evaluation between two groups
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
111
fentanyl with antiemetic drug
Asan Medical Center
Seoul, South Korea
Amount and number of postoperative analgesic requirements
Time frame: Participants will be followed for the duration of hospital stay, an expected average of 1 week
Number of participants with complications
Time frame: Up to 48 hours
Visual Analog Scale (VAS)
Time frame: Up to 48 hours
Postoperative nausea and vomiting
Time frame: Up to 48 hours
Respiratory rate, oxygen saturation
Time frame: Up to 48 hours
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