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Construction of an intelligent classification system for the mature phenotypes of cervical posterior longitudinal ligament ossification based on deep learning

Construction of an intelligent classification system for the mature phenotypes of cervical posterior longitudinal ligament ossification based on deep learning

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500114835
Enrollment
Unknown
Registered
2025-12-18
Start date
2025-12-19
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Ossification of the posterior longitudinal ligament of the cervical spine

Interventions

The immature ossification group:None
Mature ossification group:None
The non-ectopic ossification group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 35 and 70 years old, gender not restricted, and voluntarily signing the informed consent form. 2.The diagnosis was confirmed as cervical posterior longitudinal ligament ossification (the patient presented with clinical symptoms of spinal cord or nerve root damage, such as dysfunction and sensory impairment in limbs and trunk, bladder and rectum dysfunction, and pathological reflexes in limbs; X-ray or CT confirmed the presence of ectopic ossification in the posterior longitudinal ligament). The diagnosis was also confirmed as cervical spondylosis (the patient presented with clinical symptoms of spinal cord or nerve root damage, such as dysfunction and sensory impairment in limbs and trunk, bladder and rectum dysfunction, and pathological reflexes in limbs; X-ray or CT could not clearly show the presence of ectopic ossification in the posterior longitudinal ligament, and MRI showed that the spinal cord compression was of low signal intensity). 3.The symptoms and signs progressively worsened and conservative treatment was ineffective.

Exclusion criteria

Exclusion criteria: 1.Patients who have participated in other clinical trials within the past three months. 2.Congenital malformations (including but not limited to occipitocervical malformations, congenital cervical fusion, and cervical-related neurovascular malformations), cervical trauma, cervical tumors, and inflammatory diseases such as cervical tuberculosis. 3.Those with motor neuron diseases such as amyotrophic lateral sclerosis and other neurological disorders. 4.The patient's condition is poor and they cannot withstand the surgery, or the patient is not suitable for surgical treatment as determined by preoperative examinations.

Design outcomes

Primary

MeasureTime frame
Accuracy rate;Precision rate;Recall rate;

Countries

China

Contacts

Public ContactKong Qingjie

Shanghai General Hospital

15900558565@163.com+86 21 34206890

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026