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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02789774
Other study ID # USOFT
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date February 2012
Est. completion date June 2024

Study information

Verified date March 2024
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A multicenter randomized controlled trial is performed in Sweden (Uppsala, Malmo and Stockholm) comparing surgery with posterior C1-C2 fusion and conservative treatment with a rigid collar. Follow up will be performed up to one year after start of treatment registering EQ5D, NDI and cervical CT scans. Mortality will be documented during follow-up. All direct and indirect costs of treatment will be registered and used for cost-effectiveness analysis.


Description:

50 patients, based on the following calculation of study size: The standard deviation for Neck Disability index, NDI, is just under 7, while "minimally clinical important difference" (MCID) is 7 points . That gives that 16 patients are needed in each group to get 80% power with a significance level of 5%. However, in the studied population the one year mortality rate is substantial, especially after a neck injury . In order to be able to draw conclusions from the study the investigators have elected to expand the study to 25 subjects in each group. Follow up: 1w, 6w, 3m, 1y with CT, Questionaires: NDI, EQ5D. Bone density measurement at injury. Extension flexion x-ray after 1 year.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 50
Est. completion date June 2024
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender All
Age group 75 Years and older
Eligibility Inclusion Criteria: - Acute displaced odontoid fracture type II according to Anderson and D'Alonzo, age 75 years or older. Displacement defined as 4 mm anterior translator displacement, any posterior translator displacement, or 10 degrees of angulation. Exclusion Criteria: - Any contraindication to surgery, anesthesia class ASA 4 or higher (Saklad 1941), severe senile dementia (defined as being admitted to a nursing home or hospital because of the dementia), anatomical or other prerequisites that makes an operation unsuitable.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Posterior fusion C1-C2
Posterior access and screws in C1 (atlas) and C2 (axis) and fusion with addition of iliac crest bone graft. No postoperative collar.
Rigid cervical collar
External immobilization of cervical spine in a rigid collar for 12 weeks.

Locations

Country Name City State
Sweden Malmö University Hospital Malmö
Sweden Uppsala University Hospital Uppsala Uppsala County

Sponsors (1)

Lead Sponsor Collaborator
Uppsala University

Country where clinical trial is conducted

Sweden, 

References & Publications (2)

Kose et al. 2007

Olerud et al. 1999

Outcome

Type Measure Description Time frame Safety issue
Primary Neck Disability Index (NDI questionnaire) 1 year
Secondary EQ5D questionnaire 1 year
Secondary Number of participants that deceased after inclusion 1 year
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