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
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine | Bupivacaine 0.25 - 0.5% @ 4ml/hr for 72 hours |
| DRUG | Normal Saline | Normal 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.