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IV Acetaminophen in Colorectal Surgery
NCT02804633Completed
- Sponsor
- The Jewish Hospital - Mercy Health
- Start
- Aug 2013
- Primary completion
- Mar 2015
- Modality
- Small Molecules
01
Overview
Randomised, double-blind trial in postoperative pain comparing IV acetaminophen group with Placebo Group (2 arms). Primary endpoints: Total opioid consumption at 48 hours and Pain Visual Analog Scale Score at 48 hours. Started Aug 2013; status: completed.
02
Drugs
acetaminophen
03
Conditions
postoperative pain
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