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Oral Versus Intravenous Acetaminophen in Lumbar Spine Surgery

StatusNot Yet Recruiting
PhasePhase 4
Started
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Record History

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  1. Secondary endpoints: 11 to 10v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this study is to compare whether oral or intravenous acetaminophen works better for pain control in patients undergoing lumbar spine fusion surgery
Trial Details
NCT Number NCT07203079
Lead Sponsor Stanford University
Conditions
(from sponsor)		 Postoperative Pain
Related terms Postoperative Pain
Enrollment 180 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov