Acute Pain Clinical Trial
Official title:
A Phase III, Multi-Center, Open-Label, Prospective, Repeated Dose, Randomized, Controlled, Multi-Day Study of the Safety and Efficacy of Intravenous Acetaminophen in Adult Inpatients
The study will be investigating safety and efficacy administration of repeated dose of IV Acetaminophen (IV APAP) over five days for the treatment of acute pain or fever in adult patients.
• To assess the safety of IV Acetaminophen when used over five days for the treatment of
acute pain or fever in adult inpatients
Secondary Objectives:
- To compare the efficacy of IV Acetaminophen 650 milligram (mg) every four (q4) hours
vs. 1 gram (g) every 6 (q6) hours over 5 days of treatment
- To compare the safety of IV Acetaminophen 650 mg q4 hours vs. 1 g q6 hours over 5 days
of treatment
- To compare the safety of IV Acetaminophen vs. standard of care (SOC) treatment over 5
days of treatment
- To compare the efficacy of IV Acetaminophen vs. standard of care treatment over 5 days
of treatment
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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