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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
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
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Stanford University
Stanford, California, United States
Start Date
January 1, 2026
Primary Completion Date
October 1, 2026
Completion Date
January 1, 2027
Last Updated
October 8, 2025
180
ESTIMATED participants
Acetaminophen Oral Tablet
DRUG
placebo oral tablet
DRUG
Acetaminophen infusion
DRUG
Placebo infusion
DRUG
Lead Sponsor
Stanford University
NCT06862609
NCT07327463
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07436806