Comparing Surgical Decompression Versus Conservative Treatment in Incomplete Spinal Cord Injury (COSMIC)
Primary Purpose
Central Spinal Cord Syndrome
Status
Terminated
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Surgical decompression
Conservative treatment
Sponsored by
About this trial
This is an interventional treatment trial for Central Spinal Cord Syndrome focused on measuring Surgical decompression, conservative treatment, incomplete spinal cord lesion, recovery
Eligibility Criteria
Inclusion Criteria:
- all patients with a history of a traumatic event to the cervical spine fulfilling the criteria of incomplete cervical spinal cord lesion. -
Exclusion Criteria:
- cognitive impairments
- a preexistent neurologic deficit of arms and/or legs
- psychiatric illness
- significant comorbidity interfering with the indication to perform surgery or not
- use of anticoagulating drugs
- addiction to drugs or alcohol (more than five units daily)
- not speaking Dutch language fluently
- not willing to participate
- participating in another trial
Sites / Locations
- Radboud University Nijmegen Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
surgical decompression
Conservative treatment
Arm Description
surgical decompression within 24 hours post-injury
Normal conservative treatment without surgical intervention
Outcomes
Primary Outcome Measures
Dutch translation of mJOA
functional outcome at two years measured by Dutch translation of mJOA
Secondary Outcome Measures
DASH
arm/hand function assessed by the disability of the arm, shoulder and hand questionnaire (DASH)
Full Information
NCT ID
NCT01367405
First Posted
June 6, 2011
Last Updated
October 12, 2016
Sponsor
Radboud University Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01367405
Brief Title
Comparing Surgical Decompression Versus Conservative Treatment in Incomplete Spinal Cord Injury
Acronym
COSMIC
Official Title
COSMIC: Conservative or Early Surgical Management of Incomplete Cervical Cord Syndrome Without Spinal Instability. Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2013
Overall Recruitment Status
Terminated
Why Stopped
only 1 inclusion in 1.5 years due to strict exclusion criteria
Study Start Date
October 2013 (undefined)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Traumatic Central Cord Syndrome (TCCS) was until recent recognized as a separate clinical entity. The most characteristic feature is the disproportionate more motor impairment of the arms and especially the hands than the legs, bladder dysfunction and sensory.
Recently, it has been shown that the distinction of TCCS with an incomplete cervical spinal cord lesion (ICSCL) is artificial. It is the most frequent incomplete traumatic spinal cord lesion. It accounts for up to 70 % of all incomplete cervical spinal cord lesions. The exact incidence is not known.
Uncertainty about the treatment exists. A good recovery has been described after conservative treatment. Conservative treatment was usually considered when a fracture or dislocation of the spine were absent. It is often seen in hyperextension trauma in the elderly with degenerative spondylotic stenotic cervical spine. However, some reports suggest a better outcome after surgical decompression. Randomized trials have not been performed. To avoid discussion about possible confounding or effect modification related to the mechanism of trauma, this study will focus on ICSCL in patients without fracture or instability of the cervical spine on radiological examination. Also the problem of crossover from the conservative group to the surgical one due to the nature of spinal instability will be reduced.
Goal of the study: To compare the efficacy of early decompressive surgery to improve functional outcome in patients with ICSCL without a fracture or instability of the cervical spine compared to those receiving conservative treatment.
Definition of ICSCL in this study: ICSCL is an incomplete spinal cord lesion due to a cervical spine trauma. At CT scanning with reconstruction and at MRI signs are not seen that could indicate a fracture of the cervical spine or instability. An overt sequestrated herniated disc should not be present since this will always necessitate immediate surgery. Involvement of the cervical spinal cord should be established at physical examination (symptomatic arm or hand dysfunction is obligatory).
Detailed Description
See Above. Further information in this registration ( Randomized controlled trial (RCT), sample size etc)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Central Spinal Cord Syndrome
Keywords
Surgical decompression, conservative treatment, incomplete spinal cord lesion, recovery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
surgical decompression
Arm Type
Experimental
Arm Description
surgical decompression within 24 hours post-injury
Arm Title
Conservative treatment
Arm Type
Active Comparator
Arm Description
Normal conservative treatment without surgical intervention
Intervention Type
Procedure
Intervention Name(s)
Surgical decompression
Intervention Description
Surgical decompression within 24 hour postinjury
Intervention Type
Procedure
Intervention Name(s)
Conservative treatment
Intervention Description
Usual conservative treatment without surgery
Primary Outcome Measure Information:
Title
Dutch translation of mJOA
Description
functional outcome at two years measured by Dutch translation of mJOA
Time Frame
two years post-injury
Secondary Outcome Measure Information:
Title
DASH
Description
arm/hand function assessed by the disability of the arm, shoulder and hand questionnaire (DASH)
Time Frame
two years post-injury
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
- all patients with a history of a traumatic event to the cervical spine fulfilling the criteria of incomplete cervical spinal cord lesion. -
Exclusion Criteria:
cognitive impairments
a preexistent neurologic deficit of arms and/or legs
psychiatric illness
significant comorbidity interfering with the indication to perform surgery or not
use of anticoagulating drugs
addiction to drugs or alcohol (more than five units daily)
not speaking Dutch language fluently
not willing to participate
participating in another trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ronald Bartels, M.D.,Ph.D.
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500 HB
Country
Netherlands
12. IPD Sharing Statement
Citations:
PubMed Identifier
23369169
Citation
Bartels RH, Hosman AJ, van de Meent H, Hofmeijer J, Vos PE, Slooff WB, Oner FC, Coppes MH, Peul WC, Verbeek AL. Design of COSMIC: a randomized, multi-centre controlled trial comparing conservative or early surgical management of incomplete cervical cord syndrome without spinal instability. BMC Musculoskelet Disord. 2013 Jan 31;14:52. doi: 10.1186/1471-2474-14-52.
Results Reference
derived
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Comparing Surgical Decompression Versus Conservative Treatment in Incomplete Spinal Cord Injury
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