Status:
COMPLETED
NeuroVision® Dynamic Screw Test Study
Lead Sponsor:
NuVasive
Conditions:
Degenerative Spinal Conditions
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this research study is to gather information about the NeuroVision System (which is FDA cleared for this indication) during the placement of pedicle screws. NeuroVision is a machine tha...
Eligibility Criteria
Inclusion
- Male and female patients who are at least 18 years of age.
- Surgical candidates for posterior instrumented lumbar fusion surgery.
- Patients who understand the conditions of enrollment and are willing to sign an informed consent to participate in the study.
Exclusion
- Patients with underlying neurological disease or neurological deficits that are not associated with the condition for which they are seeking surgical intervention.
- Patients who have had previous instrumented surgery at the involved lumbar level.
- Participants in any other clinical study involving an investigational device or drug within 30 days of enrollment into the current study.
Key Trial Info
Start Date :
March 1 2009
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
February 1 2012
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT01232517
Start Date
March 1 2009
End Date
February 1 2012
Last Update
December 24 2025
Active Locations (3)
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1
University of California, San Francisco
San Francisco, California, United States, 94143
2
Northwest Orthopaedic Specialists, PS
Spokane, Washington, United States, 99208
3
Aurora BayCare Medical Center
Green Bay, Wisconsin, United States, 54308