Continuous Local Infusion of Anesthetic at the Incisional Site for Scoliosis Surgery
Completed · Phase 4
Conditions studied: Scoliosis
In brief
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.
Key facts
- Study ID
- NCT00508066
- Run by
- Shriners Hospitals for Children
- People needed
- 60
- Starts
- 2007-05-01
- Expected to finish
- 2011-01-01
- Last updated by the study team
- 2013-01-25
Who can join
Age: 8 and older, up to 18. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Clinical Diagnosis of Congenital Scoliosis
- Clinical Diagnosis of Idiopathic Scoliosis
- Anticipated Spinal Fusion Surgery
You may not qualify if…
- Less than 8 years of age
Where it is running
- Shriners Hospitals for Children - Los Angeles — Los Angeles, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.