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A clinical study for precise and improved spinal canal enlargement for multi-segment cervical spondylosis

A clinical study for precise and improved spinal canal enlargement for multi-segment cervical spondylosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900022363
Enrollment
Unknown
Registered
2019-04-08
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-04-15

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

Conditions

Multi-segment cervical spondylotic myelopathy

Interventions

Sponsors

The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients had clear history of symptoms and signs associated with MCSM, on whom conservative treatment had failed; (2) Patients suffered at least three compressed levels confirmed on the magnetic resonance imaging (MRI); (3) The follow-up information are complete.

Exclusion criteria

Exclusion criteria: (1) Patients acted mainly as cervical spondylotic radiculopathy (CSR) rather than myelopathy; (2) In addition to cervical disc herniation, other diseases were combined such as ossification of the posterior longitudinal ligament (OPLL), hypertrophic ligamentum flavum (HLF), fractures or tumors, etc.; (3) Patients had a history of any previous cervical spine injury or surgical intervention.

Design outcomes

Primary

MeasureTime frame
JOA;VAS;cervical alignment;operative segmental alignment;ROM;

Secondary

MeasureTime frame
operative time;blood loss;hospital stay;complication incidence;

Countries

China

Contacts

Public ContactJiang Xiaobing

The First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine

spinedrjxb@sina.com+86 13632494486

Outcome results

None listed

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