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A prospective randomized controlled study on the effect of cervical collar external fixation after the posterior double-door expansion spinal canal angioplasty

A prospective randomized controlled study on the effect of cervical collar external fixation after the posterior double-door expansion spinal canal angioplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053952
Enrollment
Unknown
Registered
2021-12-04
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-10-31

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

Conditions

Cervical degenerative disease

Interventions

Experimental group:Do not wear a cervical collar during the entire postoperative period
Control Group:Wear a neck brace throughout the surgery

Sponsors

Beijing Jishuitan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing cervical posterior double-door laminoplasty (without placing internal fixation such as microplates); 2. No history of cervical spine surgery; 3. Aged 40 to 70 years; 4. Patients with informed consent and voluntary participation.

Exclusion criteria

Exclusion criteria: 1. Subjects with severe numbness and pain in both upper extremities immediately after surgery were significantly worse than those before surgery; 2. Patients with cervical spinal cord injury caused by cervical spine trauma; 3. Patients with lumbar spine disease at the same time.

Design outcomes

Primary

MeasureTime frame
Postoperative axial symptoms;—

Secondary

MeasureTime frame
Visual Analogue Scale Score;—

Countries

China

Contacts

Public ContactLiu Mingming

Beijing Jishuitan Hospital

liuming-1619@163.com+86 18610708286

Outcome results

None listed

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