- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03355703
Anterior Odontoid Screw Osteosynthesis in Treatment of Type 2 Odontoid Fracture
Results of Anterior Odontoid Screw Osteosynthesis in Treatment of Type 2 Odontoid Fracture
Odontoid fracture is a common fracture accounting for 10-15% of all cervical fractures. It occurs in bimodal fashion in elderly and young patients.
The classification of Anderson and Alonzo provides a guide for prognosis . Type I and type III have a good rate of union, while type II has a poor prognosis due to poor blood supply. Hence, operative fixation is recommended to avoid non-union.
Treatment options for type II include anterior odontoid screw fixation and posterior C1-C2 fusion.Despite the excellent rates of bony union in posterior C1-C2 fusion, it is associated with higher morbidity, higher blood loss and significant limitation in the range of motion and rotation of the neck.the aim of the study Is to evaluate clinical and radiological outcome of anterior odontoid screw osteosynthesis in treatment of type 2 odontoid fracture.
Study Overview
Status
Conditions
Detailed Description
Preoperative evaluation:
Full clinical Evaluation and management in trauma unit using Advanced Trauma Life Support protocols.
Full neurological assessment and classification using American Spinal Injury Association score.
Radiological assessment includes antero-posterior and lateral plain cervical radiograph and CT scan for all patients. MRI will be done neurological deficit
Operative technique:
Position:
The patient is placed supine on the operating table and neck is positioned in extension so as to achieve optimum reduction. Intra-operative x-rays are obtained in the Antero_posterior and lateral planes.
Incision:
Longitudinal incision is made at the medial border of the sternomastoid muscle on the right side.The platysma is divided,and the fascia of the sternocleidomastoid is sharply incised along its medial border. Blunt dissection is used to expose the anterior surface of the spinal column at the midcervical level by opening natural planes medial to the carotid artery sheath and lateral to the trachea and esophagus.The fascia of the musculus longus colli is incised in the midline, and the muscle is elevated from the vertebra.Blunt dissection in the retropharyngeal space is used to open a tunnel in front of the vertebra to the C-2 level.
A K-wire is inserted through the incision up to the inferior edge of C-2, under Image, and impacted into the inferior edge of C-2. A K wire is advanced carefully controlled with biplane fluoroscopy from the inferior anterior edge of C-2 through the body of C-2 to the odontoid till its apex. A cannulated drill pit is then used over the wire. The drilled hole is then tapped. The screw, selected based on the measured depth, is placed and tightened firmly monitored fluoroscopically. One screw is biomechanically sufficient for fixation. The wound is checked for hemostasis,and closure completed in layers over a suction drain.
Post-operative care and follow up:
Post-operative collar for 6 weeks. Follow up visits at 2 weeks,2,6,12 months.Clinical and neurological assessment will be done and cervical X-rays will be ordered at each follow up visit.
Functional outcome will be evaluated by Association for the study of internal fixation(AO) neck pain and disability score postoperative and at 1 year follow up.
CT scan will be done for all patients at 1 year to ensure bony union.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Nag Hamady
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Assiut, Nag Hamady, Egypt, 71511
- Ahmed Mohamed Fayez ahmed
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
_ All Type II odontoid fractures in adults .
Exclusion Criteria:
- Associated fracture body of C2 .
- Reverse type of odontoid fracture pattern.
- Pathological fractures or osteoporotic bone.
- Non-union.
- Short ,kyphotic neck and obese people.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Association for the study of internal fixation(AO) neck disability index.
Time Frame: 1 year
|
AO neck disability index is a questionnaire designed to give us information as to how neck pain has affected the ability to manage in everyday life.
It consists of ten sections each of them descripes one of daily activity and graded from zero to five the higher the total score the more severity of disability.
The sections are pain intensity, personal care , lifting, reading , headache, concentration, work, driving, sleaping, recreation .
its developed by Vernon,H .&
Mior,S .
(1991)
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assesment of bony union
Time Frame: 1year
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Measured by CT scan
|
1year
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Trauma unit
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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