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Short-Term Outcomes Of Subaxial Cervical Injuries

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT05678803
Recruitment Status : Completed
First Posted : January 10, 2023
Last Update Posted : May 10, 2023
Sponsor:
Information provided by (Responsible Party):
Peter Nabil Gayed Abdelmalak, Assiut University

Brief Summary:
The subaxial cervical spine consists of levels C3 through C7 and includes both the bony anatomy as well as the ligamentous anatomy. Injuries to the subaxial cervical spine can be bony, discoligamentous or a combination of both (1). Cervical spine trauma is common resulting from high energy trauma such as falling from height and motor vehicle accident (2). Devastating sequelae of subaxial cervical spine trauma include quadriplegia, functional loss, and permanent disability

Condition or disease Intervention/treatment
Cervical Spinal Cord Injury Other: xrays and CT

Detailed Description:

Initially, all patients with subaxial cervical spine fractures require immobilization in a rigid cervical orthosis (2). Patients receiving conservative treatment are often prescribed a rigid cervical or cervicothoracic orthosis for 6 to 12 weeks with regular follow-up and interval radiographs to assess alignment.

Patients with fractures deemed unstable or neurologic compromise should undergo decompression and stabilization. Intervention within 24 hours of injury leads to better improvement in ASIA scores (3). The recent AO Spine Subaxial Classification system relies essentially on MSCT evaluation (Reference). However, MRI is superior to CT scans for evaluating the spinal cord, nerve roots, disc, and ligamentous structures in the cervical spine (4).

Even though the investigators receive and treat a large number of patients with various subaxial cervical injuries in Assiut University Hospital each year, there is no consensus about the best treatment options and uncertainty about the outcome of these treatments.

In this study, the participants will assess the short-term outcomes of all patients with subaxial cervical fractures who will be admitted to the participants' center regardless of the neurological status or treatment type used.

The participants will also create a detailed prospective database to be used for another later study on the long-term outcome

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Study Type : Observational
Actual Enrollment : 100 participants
Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Short-Term Outcomes Of Subaxial Cervical Injuries in Assiut University Trauma Center
Actual Study Start Date : March 10, 2022
Actual Primary Completion Date : March 9, 2023
Actual Study Completion Date : March 9, 2023

Resource links provided by the National Library of Medicine

Drug Information available for: X-Rays


Intervention Details:
  • Other: xrays and CT
    A dedicated sheet will be used to record patients' data including all demographic data, detailed analysis of the mechanism of injury, time of injury, time and details of surgery (if any), neurological status on admission and all radiological findings. All patients will undergo plain X-rays and CT imaging. Patients with suspected discoligamentous injuries and/or neurological deficits will also be assessed by MRI.


Primary Outcome Measures :
  1. Short-Term Outcomes Of Subaxial Cervical Injuries in Assiut University Trauma Center [ Time Frame: 1 year ]
    Neck disability index It is a standard instrument for measuring self-rated disability due to neck pain and is used by both clinicians and researchers. Each of the 10 items scores from 0 to 5. The maximum score is 50. The obtained score can be multiplied by two to produce a percentage score



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
All patients presenting with subaxial cervical spine injuries with and without cervical cord injury between January 2022 and December 2022.
Criteria

Inclusion Criteria:

  • All patients presenting with subaxial cervical spine injuries with and without cervical cord injury between January 2022 and December 2022.

Exclusion Criteria:

  • 1- Patients who refuse to participate in the study 2- Patients who are not available for 6 weeks follow up

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT05678803


Locations
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Egypt
Peternabil049@Gmail.Com
Assiut, Egypt, 71111
Sponsors and Collaborators
Assiut University
Publications:
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Responsible Party: Peter Nabil Gayed Abdelmalak, Principal investigator, Assiut University
ClinicalTrials.gov Identifier: NCT05678803    
Other Study ID Numbers: Subaxial Cervical Injuries
First Posted: January 10, 2023    Key Record Dates
Last Update Posted: May 10, 2023
Last Verified: May 2023

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Spinal Cord Injuries
Wounds and Injuries
Spinal Cord Diseases
Central Nervous System Diseases
Nervous System Diseases
Trauma, Nervous System