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Research on the Clinical Value of Using Ultra-High Field Magnetic Resonance Spinal Cord Imaging in the Diagnosis of Degenerative Cervical Myelopathy

Research on the Clinical Value of Using Ultra-High Field Magnetic Resonance Spinal Cord Imaging in the Diagnosis of Degenerative Cervical Myelopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125854
Enrollment
Unknown
Registered
2026-06-01
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Degenerative Cervical Myelopathy (DCM)

Interventions

Postoperative patient group:None
Preoperative patient group:None

Sponsors

Beijing Jishuitan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Healthy control group: (1) No symptoms or signs of spinal cord dysfunction; (2) No history of spinal cord injury or surgery; (3) Cervical MRI scan without spinal cord compression deformation; 2.DCM Postoperative patient group: A patient who underwent a posterior cervical laminoplasty at the Spinal Surgery Department of Beijing Jishuitan Hospital due to DCM, two years postoperatively; 3.DCM Preoperative patient group: (1) Patients with degenerative cervical spinal stenosis, cervical disc herniation, or ossification of the posterior longitudinal ligament in cervical degenerative diseases; (2) The symptomatic diagnosis is spinal cord type, and the nerve localization is consistent with imaging; (3) For patients who have failed formal conservative treatment and plan to undergo anterior or posterior cervical surgery; (4) No clear surgical contraindications; (5) Patient informed and agreed to enter this study; 4.Three groups common criteria: age between 40 and 70 years;

Exclusion criteria

Exclusion criteria: 1.Healthy control group: (1) Symptoms or signs of spinal cord dysfunction; (2) History of spinal cord injury or surgery; (3) Cervical MRI scan shows compression and deformation of the spinal cord; 2.DCM Postoperative patient group: (1) Acute exacerbation of spinal cord dysfunction after trauma; (2) Combined brain, thoracolumbar, or peripheral neuropathy; (3) Suspected nerve damage or C5 nerve root paralysis related to surgery; (4) Due to reasons such as metal plants and claustrophobia, 7T MRI scans cannot be performed. 3.DCM Preoperative patient group: (1) Patients with cervical traumatic fractures and dislocations or aggravated spinal cord dysfunction after trauma; (2) Cervical infectious lesions; (3) Cervical spine tumors; (4) Uncontrollable active infections exist throughout the body; (5) Surgical treatment is not allowed for other illnesses in the body; (6) Lack of autonomous behavioral ability; (7) Patients with nerve root type or mixed type, combined with severe thoracic and lumbar nerve compression or other brain, spinal cord, peripheral nerve lesions that may interfere with clinical evaluation; (8) Patients with a history of cervical spine surgery that interferes with clinical evaluation;

Design outcomes

Primary

MeasureTime frame
7 Tesla magnetic resonance imaging;abbreviated as JOA score;

Secondary

MeasureTime frame
10-Second Finger Clench-Extension Test;Triangle step test, 10-second step-in-place test;Subjective symptoms or objective signs of spinal cord dysfunction;

Countries

China

Contacts

Public ContactXiao Han

Beijing Jishuitan Hospital, Capital Medical University

hanxiaomd@vip.163.com+86 10 5851 6934

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026