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Clinical trial

A Double-blind Randomized, Placebo-controlled Study to Determine the Effectiveness of Pre-operative IV Acetaminophen Administration in Reducing Post-operative Pain, Nausea, and Vomiting in the Outpatient Setting

NCT02102555 is registered in ClinicalTrials.gov with MercyOne Des Moines Medical Center as lead sponsor.

NCT NCT02102555
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Registry record

As filed in ClinicalTrials.gov.

Title
A Double-blind Randomized, Placebo-controlled Study to Determine the Effectiveness of Pre-operative IV Acetaminophen Administration in Reducing Post-operative Pain, Nausea, and Vomiting in the Outpatient Setting
Lead sponsor
MercyOne Des Moines Medical Center
Phase
Phase 3
Overall status
Terminated
Start date
October 31, 2013
Completion date
May 3, 2017
Enrollment
82 (actual)
Sites
1

Conditions

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

post operative nausea and vomiting, post operative pain