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Application of 3D printed titanium metal bone trabecular atlantoaxial lateral block fusion device in upper cervical spondylosis

Application of 3D printed titanium metal bone trabecular atlantoaxial lateral block fusion device in upper cervical spondylosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113239
Enrollment
Unknown
Registered
2025-11-26
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

upper cervical spondylosis

Interventions

3D printed titanium metal bone trabecular fusion device group:None
PEEK Fusion Device Group:None

Sponsors

The First Affiliated Hospital of PLA Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with upper cervical spine deformity (atlantoaxial dislocation, basilar depression); 2. Treated via posterior atlantoaxial reduction and fusion with internal fixation; 3. Lateral fusion blocks utilised 3D-printed titanium trabecular bone fusion cages or PEEK fusion cages; 4. Atlantoaxial facet joints present, with no evidence of robust bony fusion; 5. Complete medical records available.

Exclusion criteria

Exclusion criteria: 1. Spinal infection, tumour, or tuberculosis; 2. Traumatic injury; 3. History of posterior cervical spine surgery; 4. Cases unsuitable for fusion device placement due to inability to assume prone position (e.g., advanced age, critical condition), severe osteoporosis, or localised infection; 5. Follow-up duration < 24 months; 6. Missing imaging data or loss to follow-up.

Design outcomes

Primary

MeasureTime frame
atlantodental interval;cervicomedullary angle;

Secondary

MeasureTime frame
JOA score ;VAS score;

Countries

China

Contacts

Public ContactLi Mo

The First Affiliated Hospital of PLA Air Force Medical University

limo0729@hotmail.com+86 137 7202 8397

Outcome results

None listed

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