Actively Recruiting

Age: 18Years - 100Years
All Genders
ID05446259

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

Age: 18Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of degenerative cervical myelopathy
  • Diagnosis of cervical degenerative disease without myelopathy
  • Age between 18 and 100 years
Not Eligible

You will not qualify if you...

  • None outside diagnostic requirements and age limits

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Monitoring

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

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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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