Clinical Trials Directory

Trials / Unknown

UnknownNCT02067442

Prospective, Randomized, Double Blind Study Comparing IV vs PO Acetaminophen in Patients Undergoing Lumbar Discectomy

Prospective, Randomized, Double-blind, Placebo-Controlled Study to Compare the Effects of Intravenous Versus Oral Acetaminophen on Postoperative Clinical Outcomes After Ambulatory Lumbar Discectomy

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Thomas Jefferson University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Both intravenous and oral acetaminophen have been shown to reduce post-operative pain scores when given preoperatively. This study investigates if there is a difference between the intravenous and the oral forms when given preoperatively to patients undergoing lumbar microdiscectomy. We hypothesize that the intravenous formulation does not improve pain scores or decrease opioid consumption during the first postoperative day compared to the oral formulation.

Conditions

Interventions

TypeNameDescription
DRUGoral acetaminophen1000 milligrams given orally before surgery
DRUGintravenous acetaminophen1000 milligrams of intravenous acetaminophen given before surgery

Timeline

Start date
2013-08-01
Primary completion
2015-07-01
First posted
2014-02-20
Last updated
2015-03-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02067442. Inclusion in this directory is not an endorsement.