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Clinical trial

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

NCT02244619 is registered in ClinicalTrials.gov with Kettering Health Network as lead sponsor.

NCT NCT02244619
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Registry record

As filed in ClinicalTrials.gov.

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
Lead sponsor
Kettering Health Network
Phase
Phase 4
Overall status
Completed
Start date
September 30, 2014
Completion date
April 30, 2016
Enrollment
515 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

post-op pain