Actively Recruiting

Age: 18Years - 60Years
All Genders
ID06971575

Cervical Radiculopathy Imaging Using MR Neurography With Electrodiagnostic Correlation

Led by Hospital for Special Surgery, New York · Updated on 2026-04-27

20

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying patients with cervical radiculopathy, a condition involving nerve issues in the neck area. This observational project aims to assess the diagnostic and prognostic value of magnetic resonance neurography (MRN), electrodiagnostic (EDX) studies, and clinical history and physical exam findings. The study will explore how these data separately or together relate to patient responses to procedural and non-procedural treatments. Participants diagnosed with unilateral cervical radiculopathy and clinical weakness will undergo specialized cervical MRI scans with magnetic resonance neurography sequences to examine nerve roots outside the spinal canal. Electrodiagnostic testing results will also be included if performed prior to surgery. The study focuses on patients with symptom onset between 2 and 12 weeks and MRI findings showing radiculopathy, with or without spinal cord compression. During the study, researchers will collect baseline imaging and electrodiagnostic data, then assess pain levels and neck disability at baseline, 3 months, 6 months, and 12 months. Outcomes measured include nerve abnormalities on MRN imaging and their relationship to electrodiagnostic findings. Participants will be monitored over time to better understand the correlations between diagnostic tools and treatment responses. The study is sponsored by the Hospital for Special Surgery, New York, and runs until October 2026.

CONDITIONS

Brief Title

Cervical Radiculopathy Imaging Using MRN With Electrodiagnostic Correlation

Who Can Participate

Age: 18Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting with symptoms compatible with acute or subacute unilateral (one-sided) cervical radiculopathy and signs of clinical weakness
  • 18-60 years old at the time of evaluation
  • Symptom onset of 2 to 12 weeks leading up to baseline visit
  • Diagnosis of unilateral cervical radiculopathy, with or without spinal cord compression, based on signs and symptoms, physical exam and supported by MRI findings of radiculopathy (as evidenced by foraminal stenosis/narrowing) based on standard-of-care cervical spine MRI
  • Patients who have undergone or have planned electrodiagnostic testing at HSS prior to surgery
Not Eligible

You will not qualify if you...

  • Prior cervical surgery or instrumentation
  • Those who have had a prior episode of cervical radiculopathy
  • History of peripheral neuropathy or another acute or chronic neurodegenerative condition
  • History of stroke, cerebellar disease, or central nervous system disease
  • Contraindications to undergoing a standard MRI examination (e.g., pregnancy)
  • Patients presenting with bilateral cervical radiculopathy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline visit

Participants undergo cervical magnetic resonance neurography (MRN) and electrodiagnostic testing to evaluate cervical nerve roots and correlate imaging findings.

1 visit (in-person)

Long-term Monitoring

Duration - 12 months

Participants are followed to assess pain and neck disability over time using surveys at multiple timepoints.

Visits at 3 months, 6 months, and 12 months (in-person or remote)

Trial Site Locations

Total: 1 location

1

Hospital for Special Surgery

New York, New York, United States, 10021

Actively Recruiting

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Research Team

J

J. Levi Chazen, MD

C

Carlo Milani, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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