Actively Recruiting
Development of a Predictive Outcome Model for Patients With Degenerative Cervical Myelopathy Using Functional and Biological Measures
Led by Francis Farhadi · Updated on 2026-02-13
245
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are creating a research repository including patients diagnosed with degenerative cervical myelopathy (DCM) and a control group of individuals with cervical spinal disease but no myelopathic symptoms. This repository aims to study functional and biological measures to better predict symptom progression and treatment responses in DCM patients. The study also seeks to develop a risk assessment scale to forecast functional outcomes after surgery for DCM. Participants will be grouped into those with diagnosed DCM and those with cervical spinal disease without myelopathy. The study involves collecting standard clinical care data such as surgical interventions, imaging results, laboratory findings, and outcome measurements. These data will be analyzed to compare DCM patients to controls and to build predictive models. During the study, participants will undergo routine clinical assessments and standard care procedures as part of their treatment. Researchers will monitor and compare data between the DCM and control groups over a two-year period. This observational study does not involve experimental treatments but focuses on gathering detailed clinical information to understand disease progression and outcomes better.
CONDITIONS
Brief Title
Degenerative Cervical Myelopathy Repository
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of degenerative cervical myelopathy
- Diagnosis of cervical degenerative disease without myelopathy
- Age between 18 and 100 years
You will not qualify if you...
- None outside diagnostic requirements and age limits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 2 years
Participants who undergo routine care are observed with data collected from standard clinical care procedures and outcome measurements.
Data collection during standard clinical care visits over 2 years
Trial Site Locations
Total: 1 location
1
University of Kentucky
Lexington, Kentucky, United States, 40536
Actively Recruiting
Research Team
F
Francis Farhadi, MD, PhD
H
Harshit Arora, PhD
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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