Evaluating imaging techniques for cervical radiculopathy
Cervical Radiculopathy Imaging Using MR Neurography With Electrodiagnostic Correlation
This study is testing how well MRI and nerve tests can help doctors understand and treat people with neck pain caused by nerve issues.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Hospital for Special Surgery, New York Academic / other |
| Locations | 1 site (New York, New York) |
| Trial ID | NCT06971575 on ClinicalTrials.gov |
What this trial studies
This project investigates patients with cervical radiculopathy by assessing the diagnostic and prognostic value of magnetic resonance neurography (MRN) and electrodiagnostic studies. The study aims to determine how these imaging techniques, along with clinical history and physical examination findings, correlate with treatment responses. By analyzing data from these methods, the research seeks to enhance understanding of cervical radiculopathy and improve patient outcomes. The study is observational and focuses on patients experiencing acute or subacute symptoms.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-60 with acute or subacute unilateral cervical radiculopathy symptoms and clinical weakness.
Not a fit: Patients with prior cervical surgery, previous episodes of cervical radiculopathy, or other significant neurological conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnostic accuracy and treatment strategies for patients with cervical radiculopathy.
How similar studies have performed: While the specific combination of MRN and electrodiagnostic studies in this context may be novel, similar imaging approaches have shown promise in diagnosing and managing radiculopathy in other studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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 Exclusion Criteria: * 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
Where this trial is running
New York, New York
- Hospital for Special Surgery — New York, New York, United States (Recruiting)
Study contacts
- Study coordinator: J. Levi Chazen, MD
- Email: chazenjl@hss.edu
- Phone: 212-774-7149
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.