Personalized Spine Study Group (PSSG) Registry of Patients With Personalized Spine Rod Implantation
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY
The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 10
Maximum Age: 85
Healthy Volunteers: f
View:
• Patient has been/ will be operated and instrumented with patient-specific rod or spine hardware (control cohort)
• Patient able to consent or assent
Locations
United States
Colorado
Dr. Christopher Kleck, MD
RECRUITING
Aurora
Contact Information
Primary
Christopher Kleck, MD
Christopher.Kleck@CUAnschutz.edu
720-848-1900
Backup
jiandong hao
jiandong.hao@cuanschutz.edu
303-724-7457
Time Frame
Start Date: 2020-10-29
Estimated Completion Date: 2030-04
Participants
Target number of participants: 1000
Treatments
Patients with Personalized SpineRods
The patient is being treated with the patient-specific rod with a surgery date planned
Patient with other hardware
Patients with other hardware not patient-specific
Related Therapeutic Areas
Sponsors
Collaborators: Personalized Spine Study Group
Leads: University of Colorado, Denver