Skip to main content
Clinical Trials/NCT01978847
NCT01978847
Completed
Not Applicable

Proposal for Retrospective Review of Anterior&Posterior Cervical, Thoracic, and Lumbar Instrumented Arthrodesis Surgeries Performed at OSU.

H Francis Farhadi, MD, PhD1 site in 1 country500 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Condition
Sponsor
H Francis Farhadi, MD, PhD
Enrollment
500
Locations
1
Primary Endpoint
The number of patients with radiologic evidence of fusion
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Retrospective review will allow for an evaluation of potential patient- or procedure-related factors that are associated with the development of either radiologic or clinical adjacent-segment pathology.

Detailed Description

Spinal arthrodesis can be performed through either anterior, posterior, or lateral approaches for a variety of traumatic, degenerative, or deformity conditions. In recent years, the development of more sophisticated segmental instrumentation techniques and hardware has allowed for incorporation of multiple spinal levels in single settings. The long-term consequences for spinal motion segments adjacent to such fusions remain unknown. The investigators propose to undertake a retrospective case study analysis evaluating both radiologic and clinical parameters indicative of adjacent-segment pathology in patients who have undergone instrumented arthrodesis procedures at Ohio State University, performed by either Dr. Francis Farhadi, James B. Elder, or Gary Rea.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
May 1, 2018
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
H Francis Farhadi, MD, PhD
Responsible Party
Sponsor Investigator
Principal Investigator

H Francis Farhadi, MD, PhD

Assistant Professor

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • Must have had a Spinal arthrodesis procedure at Ohio State University

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

The number of patients with radiologic evidence of fusion

Time Frame: 5 years

Radiologic review will include X-Rays, CT, and MRI at pre-surgery, as well as X-rays at 6 weeks, 3, 6, 12, 24, 36, 48 and 60 months post-operatively.

Secondary Outcomes

  • The number of patient with clinical evidences of fusions(5 years)

Study Sites (1)

Loading locations...

Similar Trials