HD Research LLC | First Surgical Hospital
Status and phase
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About
The purpose of this study is to evaluate effectiveness of a fixed combination of acetaminophen/naproxen sodium compared with placebo for reduction of pain when administered as multiple doses over a 48-hour period.
Enrollment
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Volunteers
Inclusion criteria
Postoperative Inclusion Criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
122 participants in 2 patient groups, including a placebo group
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Central trial contact
Kenvue GCO Clinical Mailbox
Data sourced from clinicaltrials.gov
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