Clinical Trials Directory

Trials / Completed

CompletedNCT00508066

Continuous Local Infusion of Anesthetic at the Incisional Site for Scoliosis Surgery

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Shriners Hospitals for Children · Academic / Other
Sex
All
Age
8 Years – 18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the effects of continuous local anesthetic delivery on the immediate post-op recovery of patients undergoing spinal fusion surgery for congenital or idiopathic scoliosis.

Detailed description

Constant local analgesic infusion is a relatively new modality that provides a constant supply of medication without the need for repeat injections. This method has shown encouraging results with respect to pain levels, narcotic use, faster rehabilitation and shorter hospital stay in patients undergoing laparotomies, iliac crest bone graft harvest, and sternotomies. In addition, there have not been any reported complications when used in these scenarios. We hope to confirm better pain control, less narcotic use (i.e. PCA), fewer narcotic side effects, better response to physical therapy and earlier discharge. Which may be generalized to the spinal surgery patient population as less pain and suffering and a better overall hospital course

Conditions

Interventions

TypeNameDescription
DRUGBupivacaineBupivacaine 0.25 - 0.5% @ 4ml/hr for 72 hours
DRUGNormal SalineNormal Saline, 4ml/hour for 72 hours.

Timeline

Start date
2007-05-01
Primary completion
2011-01-01
Completion
2011-01-01
First posted
2007-07-27
Last updated
2013-01-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00508066. Inclusion in this directory is not an endorsement.