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Clinical trial

A Randomized, Double-Blind, Placebo-Controlled Trial Comparing 48-Hour Post-Operative Administration of Oral Versus Intravenous Acetaminophen in Patients Undergoing Lumbar Spine Fusion Surgery

NCT07203079 is registered in ClinicalTrials.gov with Stanford University as lead sponsor.

NCT NCT07203079
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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-Blind, Placebo-Controlled Trial Comparing 48-Hour Post-Operative Administration of Oral Versus Intravenous Acetaminophen in Patients Undergoing Lumbar Spine Fusion Surgery
Lead sponsor
Stanford University
Phase
Phase 4
Overall status
Not yet recruiting
Start date
January 31, 2026
Completion date
January 31, 2027
Enrollment
180 (estimated)
Sites
1

Conditions

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

postoperative pain