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A comparison of C3-C7 laminoplasty and C4-C7 laminoplasty with C3 laminectomy: a single institution, single blinded, randomized controlled clinical trial

A comparison of C3-C7 laminoplasty and C4-C7 laminoplasty with C3 laminectomy: a single institution, single blinded, randomized controlled clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026132
Enrollment
Unknown
Registered
2019-09-23
Start date
2019-09-24
Completion date
Unknown
Last updated
2019-09-30

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

Conditions

cervical spondylosis

Interventions

C4-C7 laminoplasty with C3 laminectomy:C4-C7 laminoplasty with C3 laminectomy
C3-C7 laminoplasty:C3-C7 laminoplasty

Sponsors

Affiliated Drum Tower Hospital, Medical School of Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with multi-level (>=3) cervical spinal cord compression and corresponding symptoms and/or signs requiring posterior decompression surgery; 2. Age between 18 and 80 years; 3. Written informed consent was obtained.

Exclusion criteria

Exclusion criteria: 1. Trauma, infection or tumor of the cervical spine; 2. History of cervical spine surgery; 3. Posterior cervical fixation with screw-rod system; 4. Combined anterior and posterior cervical spine surgery.

Design outcomes

Primary

MeasureTime frame
spontaneous fusion rate of C2-C3;

Secondary

MeasureTime frame
VAS score of neck and upper limb pain;cervical range of motion;NDI score;JOA score;SF-36;compression severity of cervical spinal cord;diameter of cervical spinal canal;

Countries

China

Contacts

Public ContactBangping Qian

Affiliated Drum Tower Hospital, Medical School of Nanjing University

qianbangping@163.com+86 13951680106

Outcome results

None listed

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