Geneva, Oct. 21 -- International Clinical Trials Registry received information related to the study (NCT07203079) titled 'Oral Versus Intravenous Acetaminophen in Lumbar Spine Surgery' on Sept. 24.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator).
Primary Sponsor: Stanford University
Condition:
Postoperative Pain
Intervention:
Drug: Acetaminophen Oral Tablet
Drug: placebo oral tablet
Drug: Acetaminophen infusion
Recruitment Status: Not recruiting
Phase: Phase 4
Date of First Enrollment: January 2026
Target Sample Size: 180
Countries of Recruitment:
United States
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