Trials / Completed
CompletedNCT00510575
Surgical Outcomes Using Variable Rod Diameters in the Treatment of Idiopathic Scoliosis
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 300 (actual)
- Sponsor
- Shriners Hospitals for Children · Academic / Other
- Sex
- All
- Age
- 11 Years – 18 Years
- Healthy volunteers
- Not accepted
Summary
There are two rod sizes routinely used for the correction of juvenile and adolescent idiopathic scoliosis, 5.5mm and 6.35mm, typically stainless steel. Currently there is no scientific evidence supporting the superiority of one size rod relative to the other. This study will evaluate the amount of radiographic correction obtained using the 5.5mm versus the 6.35mm spinal instrumentation rods.
Detailed description
For the correction of Juvenile and Adolescent idiopathic scoliosis, companies offer and surgeons use varying rod sizes not based on scientific evidence, but because of personal preference, availability and company loyalty. To date there has been no literature evaluating the benefit or harm of one rod size versus the other. Our dual-arm prospective study will evaluate the amount of radiographic correction obtained using the 5.5mm versus the 6.35mm stainless steel instrumentation rods. These are both standard rods used in the community for this particular procedure, thus no additional risk exists for the patient. The results of this study will help guide surgeons in their decision making process when faced with the multitude of options offered by implant manufactures. Comparison(s): 5.5mm stainless steel spinal rod versus 6.35mm stainless steel spinal rod for correction of juvenile and idiopathic scoliosis curves.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Spinal rod | Posterior spinal fusion using a 5.5 or 6.35 size rod |
Timeline
- Start date
- 2007-05-01
- Primary completion
- 2011-01-01
- Completion
- 2011-01-01
- First posted
- 2007-08-02
- Last updated
- 2013-01-16
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00510575. Inclusion in this directory is not an endorsement.