drugset / Trial / NCT02061774

Postoperative Opioid Use and Pain Scores in Patients Undergoing Transforaminal Lumbar Interbody Fusion

NCT02061774 ↗

Phase 4 Terminated 21 enrolled Texas Tech University Health Sciences Center
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this project is to study the effects of preoperative followed by scheduled intravenous acetaminophen on pain control for 24 hours postoperatively after minimally invasive 1 or 2 level transforaminal lumbar interbody fusion.

Timeline

Start
2013-10
Primary completion
2018-01-11
Completion
2018-01-11

Outcome

Outcome not reported

Stopped: “Preliminary analysis showed not clinically significant. Study ended and closed 1/11/2018”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Acetaminophen Small molecule 1 g Intravenous

Indications

No indication recorded.