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Clinical Trial Summary

This study aimed to evaluate the additive effect of acetaminophen on postoperative pain control in patients receiving nefopam and fentanyl-based patient-controlled analgesia. Participants undergoing laparoscopic hysterectomy will be randomly assigned to treatment group or control group. After end of surgery, acetaminophen or normal saline (placebo) will be administered intravenously depending on the group assigned.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03644147
Study type Interventional
Source Seoul National University Hospital
Contact
Status Completed
Phase N/A
Start date August 27, 2018
Completion date January 7, 2021

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