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A bidirectional cohort study of posterior cervical surgery with cervical function-preserving

A bidirectional cohort study of anterior/posterior cervical surgery with cervical function-preserving

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089848
Enrollment
Unknown
Registered
2024-09-18
Start date
2023-01-10
Completion date
Unknown
Last updated
2024-09-23

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

Conditions

Degenerative cervical myelopathy

Interventions

Group Bryan CDA:NA
Group ProDisc-C CDA:NA
Group Laminoplasty with preserving unilateral muscle-ligament complex:NA
Gruop modiified laminoplasty:NA

Sponsors

Peking Univversity Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients who had undergone Bryan and ProDisc-C cervical artificial disc replacement, laminoplasty with preservation of unilateral muscle-ligament complex, and modified laminoplasty through the intermuscular approach in Peking University Third Hospital from December 2003.

Exclusion criteria

Exclusion criteria: 1. Patients who had undergone secondary or more cervical spine surgeries, including anterior or posterior cervical surgeries; 2. Patients who had undergone combined anterior and posterior cervical surgery; 3. Patients with concomitant tumors, tuberculosis, and trauma; 4. Patients with preoperative active infections; 5. Patients who had undergonewho had missing clinical data, including demographic data, imaging data, surgical related data, etc; 6. Patients who had lost to follow-up.

Design outcomes

Primary

MeasureTime frame
modified Japanese Orthopedics Association score;Visual Analogue Scale score;

Secondary

MeasureTime frame
Neck Disability Index;Cervical Range of motion;C2-C7 Cervical Sagittal Vertical Axis;T1 Slope;

Countries

Chnia

Contacts

Public ContactZhou Feifei

Peking Univversity Third Hospital

orthozhou@163.com+86 135 8178 7350

Outcome results

None listed

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