Actively Recruiting
Personalized Spine Study Group (PSSG) Registry
Led by University of Colorado, Denver · Updated on 2024-10-03
1000
Participants Needed
1
Research Sites
491 weeks
Total Duration
On this page
Sponsors
U
University of Colorado, Denver
Lead Sponsor
P
Personalized Spine Study Group
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Personalized Spine Study Group (PSSG) Registry
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient has been or will be operated on and instrumented with a patient-specific rod or spine hardware (control group)
- Patient is able to give consent or assent
You will not qualify if you...
- Patient is unable to sign an informed consent form
- Patient is unable to complete a self-administered questionnaire
- Patient is pregnant or plans to become pregnant during the study
- Patient is older than 85 years
- Patient is younger than 10 years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Dr. Christopher Kleck, MD
Aurora, Colorado, United States, 80045
Actively Recruiting
Research Team
C
Christopher Kleck, MD
CONTACT
J
jiandong hao
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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