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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02788760
Other study ID # 2016/332
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date June 2016
Est. completion date April 2018

Study information

Verified date March 2020
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Most fractures of the cervical spine are considered stable and treated with a rigid cervical collar. However no studies have to date been published addressing the length of treatment. There seems to be a significant dissimilarity between hospitals within and between countries with the length of collar treatment varying from 6 to 12 weeks. At the neurosurgical department at Oslo University Hospital, Ullevål the standard length of treatment for a stable cervical fracture is 12 weeks. This study seeks to establish whether 6 weeks of collar treatment for a specific subtype of stable fractures in the cervical spine is sufficient.


Description:

The investigators will include 150 patients with a stable cervical fractures of vertebra C3-C7 with a Subaxial Cervical Spine Injury Severity (SLIC) Score 1-3 and randomize them in to two similar groups. One group will be treated with a cervical collar for 6 weeks and the other group will be treated for 12 weeks. There will be a clinical check up and a CT scan at 1, 6, 12 and 26 weeks after the initial injury. The investigators will compare the results between the two groups when it comes to fracture healing (CT based), level of function, pain and the length of sick leave with a total of 6 months of follow up.


Recruitment information / eligibility

Status Terminated
Enrollment 32
Est. completion date April 2018
Est. primary completion date April 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Patients with a newly diagnosed (within 5 days of injury) fracture in vertebra C3-C7 with SLIC score 1-3

- Patients must be abel to give their consent to participate in the study

Exclusion Criteria:

- Unstable cervical fractures in need of surgery

- SLIC score >3

- Fractures of the spinous process and the transverse process in the cervical spine

- Stable fractures in in the C3-C7 vertebra combined with fractures of the C0-C2 vertebra

- Pathological fractures in the cervical spine

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Cervical collar (Miami J collar - Össur)
The two groups of patients will similar in every way and will be treated with the same type of cervical collar - the only difference will be the length of treatment

Locations

Country Name City State
Norway Neurosurgical department, Oslo university hospital, Ullevål Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fracture healing The fracture healing will be assessed based on CT scans at 6 months 6 months
Primary Visual analogue scale - neck pain and radiculopathy Pain will be assessed at 6 months based on the Visual Analogue Scale and the use of pain medication will be recorded at 6 months 6 months
Secondary Level of function Level of function will be assessed at 6 months using the Neck Disability Index and the Karnofsky Performance Scale Index and by registering the length of sick leave at 6 months 6 months
Secondary Treatment failure Treatment failure will be recorded in both arms at 6 months. Defined as the need for surgery in both groups or the need to extend the use of collar from 6 to 12 weeks in the 6 weeks group 6 months