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Degenerative Cervical Myelopathy Repository

Recruiting
Conditions
Cervical Myelopathy
Interventions
Other: Standard clinical care procedures and outcome measurements.
Registration Number
NCT05446259
Lead Sponsor
University of Kentucky
Brief Summary

To create a research repository of patients with known degenerative cervical myelopathy (DCM) and a control cohort of subjects who have non-myelopathic spinal disease. This repository will be used to assess functional and/or biological measures that may allow for improved prediction of symptomatic progression and response to treatment in patients with DCM. In addition, this repository will be used to develop a risk assessment scale to accurately predict functional outcomes following operative management of DCM.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
245
Inclusion Criteria
  • Diagnosis of degenerative cervical myelopathy
  • Diagnosis of cervical degenerative disease without myelopathy
Exclusion Criteria
  • None outside or diagnostic requirements and age limits.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Control groupStandard clinical care procedures and outcome measurements.Subjects diagnosed with cervical spinal disease without myelopathic symptoms.
DCM groupStandard clinical care procedures and outcome measurements.Subjects diagnosed with degenerative cervical myelopathy.
Primary Outcome Measures
NameTimeMethod
Data comparison between DCM and control groups2 years

This study is to determine biomarkers associated with DCM and analyze objective clinical measures to determine more predictable and potentially effective treatments for patients diagnosed with cervical myelopathy.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Kentucky

🇺🇸

Lexington, Kentucky, United States

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