Post-op Pain Clinical Trial
Official title:
Randomized, Double-Blind, Study Comparing Oral Acetaminophen Plus Intravenous (IV) Placebo to Oral Placebo Plus IV Acetaminophen Given Perioperatively for Controlling Pain in the 24hr Post-op Period After Total Hip or Knee Joint Replacement
The purpose of the study is to evaluate post-op pain requirements in patients undergoing hip or knee replacement surgery who perioperatively receive either Oral acetaminophen or IV acetaminophen
Subjects will be randomized to receive perioperative dosing of either:
1. Oral acetaminophen (Tylenol) 1000mg with IV Placebo (100ml Normal Saline), OR,
2. IV acetaminophen (Ofirmev) 1000mg/100ml with Oral Placebo (oral capsules).
Subject pain levels and post-operative opioid use will be tracked for up to 24 hours after
surgery.
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Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
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N/A | |
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