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

Stopped early · Phase 4 · Has a placebo group

Conditions studied: Low Back Pain

In brief

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.

Key facts

Study ID
NCT02061774
Run by
Texas Tech University Health Sciences Center
People needed
21
Starts
2013-10-01
Expected to finish
2018-01-11
Last updated by the study team
2020-05-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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