Status:
NOT_YET_RECRUITING
Oral Versus Intravenous Acetaminophen in Lumbar Spine Surgery
Lead Sponsor:
Stanford University
Conditions:
Postoperative Pain
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
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
Eligibility Criteria
Inclusion
- Plan for open lumbar laminectomy and fusion surgery (1-3 levels)
- Able to provide written informed consent
- Must be able to swallow pills
Exclusion
- Medical contraindications to acetaminophen
- Emergency surgery
- Chronic pain unrelated to surgery
- Pregnancy
Key Trial Info
Start Date :
January 1 2026
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
January 1 2027
Estimated Enrollment :
180 Patients enrolled
Trial Details
Trial ID
NCT07203079
Start Date
January 1 2026
End Date
January 1 2027
Last Update
October 8 2025
Active Locations (1)
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1
Stanford University
Stanford, California, United States, 94305