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A prospective, randomized, placebo controlled, double-blinded study at a single institution.
Pain medicine literature and the principal investigator's anecdotal experience in posterior cervical and lumbar instrumented spine surgery suggest that pre-incisional IV ibuprofen significantly reduces postoperative pain without increasing surgical complications or fusion rate, which leads to earlier ambulation, less dependence on narcotic medications, shorter hospital stays, and earlier return to work. The purpose of this study is to assess if these anecdotal findings hold true in a randomized clinical trial of patients with cervical or lumbar spondylosis, who are undergoing decompression and instrumented fusion of the spine.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
SJHMC/Barrow Neurosurgical Associates
Phoenix, Arizona, United States
Start Date
March 1, 2015
Primary Completion Date
June 1, 2017
Completion Date
July 17, 2017
Last Updated
April 19, 2024
6
ACTUAL participants
Ibuprofen
DRUG
normal saline
OTHER
Lead Sponsor
St. Joseph's Hospital and Medical Center, Phoenix
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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