RECRUITING

Cervical Radiculopathy Imaging Using MRN With Electrodiagnostic Correlation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This project will study patients with cervical radiculopathy. We will evaluate the combined diagnostic and prognostic value of magnetic resonance neurography (MRN), electrodiagnostic (EDX) studies, and historical and physical clinical elements. Specifically, this project will explore whether these data individually or in combination correlate with response to procedural and non-procedural treatment.

Official Title

Cervical Radiculopathy Imaging Using MR Neurography With Electrodiagnostic Correlation

Quick Facts

Study Start:2023-10-24
Study Completion:2026-03
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06971575

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients presenting with symptoms compatible with acute or subacute unilateral (one-sided) cervical radiculopathy and signs of clinical weakness
  2. * 18-60 years old at the time of evaluation
  3. * Symptom onset of 2 to 12 weeks leading up to baseline visit
  4. * 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
  5. * Patients who have undergone or have planned electrodiagnostic testing at HSS prior to surgery
  1. * Prior cervical surgery or instrumentation
  2. * Those who have had a prior episode of cervical radiculopathy
  3. * History of peripheral neuropathy or another acute or chronic neurodegenerative condition
  4. * History of stroke, cerebellar disease, or central nervous system disease
  5. * Contraindications to undergoing a standard MRI examination (e.g., pregnancy)
  6. * Patients presenting with bilateral cervical radiculopathy

Contacts and Locations

Study Contact

J. Levi Chazen, MD
CONTACT
212-774-7149
chazenjl@hss.edu
Carlo Milani, MD
CONTACT
milanic@hss.edu

Study Locations (Sites)

Hospital for Special Surgery
New York, New York, 10021
United States

Collaborators and Investigators

Sponsor: Hospital for Special Surgery, New York

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-10-24
Study Completion Date2026-03

Study Record Updates

Study Start Date2023-10-24
Study Completion Date2026-03

Terms related to this study

Additional Relevant MeSH Terms

  • Cervical Radiculopathy