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Evaluation of clinical safety and efficiency of ultrasonic bone curette used in anterior cervical discectomy and fusion surgery

Evaluation of clinical safety and efficiency of ultrasonic bone curette used in anterior cervical discectomy and fusion surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089852
Enrollment
Unknown
Registered
2024-09-18
Start date
2022-05-01
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

Cervical spondylotic myelopathy

Interventions

New Technology Group:Using ultrasonic bone curette
Control Group:Using traditional tools

Sponsors

Luohe Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed as cervical spondylotic myelopathy, there are clinical manifestations and signs of cervical spinal cord compression, such as upper limb numbness and pain, decreased muscle strength of limbs, positive pathological signs, etc.; (2) Cervical disc herniation and/or osteophytes at the posterior margin of the vertebral body were limited to one segment; (3) Isolated ossification of the posterior longitudinal ligament is confined to the level of the intervertebral space at 1 segment; (4) The operative space was between C3/4 and C6/7. (5)Patients undergoing zero-notch interbody fusion (ZERO-P) internal fixation.

Exclusion criteria

Exclusion criteria: (1) Multi-segment cervical disc protrusion; (2) Ossification of the posterior longitudinal ligament was more than one segment, requiring subtotal vertebral resection; (3) Patients with a history of cervical spine surgery; (4) Cervical tumor patients; (5) Cervical vertebra injury.

Design outcomes

Primary

MeasureTime frame
JOA score;Spinal canal invasion rate;

Secondary

MeasureTime frame
Duration of surgery;

Countries

China

Contacts

Public ContactYuwei Li

Staff of Luohe Central Hospital

460910316@qq.com+86 139 4986 8369

Outcome results

None listed

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