Association of Quantitative and Functional Imaging With Clinical Outcome After Spinal Cord Injury

Swiss Paraplegic Research, Nottwil57 enrolled

Overview

The overall study aim is to provide additional magnetic resonance imaging parameters of the cervical spinal cord, brainstem and brain and a better understanding of changes after spinal cord injury (SCI) and to define new magnetic resonance (MR) biomarkers to correlate with sensomotoric functioning and clinical outcome.

Injury of the spinal cord, for instance induced by trauma, is complex involving primary mechanisms caused by forces directly affecting the spinal cord and secondary mechanisms consisting of complex physiological processes after trauma. Conventional magnetic resonance imaging (MRI) is the current standard to assess morphologic changes of the spinal cord after injury. However, conventional MRI provides little information regarding the health and integrity of the brain and spinal cord tissue itself, due to the fact that signal intensity changes are non-specific and do not correspond directly with physiological processes. This is reflected in the poor correlation of conventional MRI data with neurological and functional impairment in various spinal cord pathologies (such as multiple sclerosis compression myelopathy) and failure to provide reliable prognostic information. By applying a combination of diffusion weighted imaging, functional MRI and magnetic resonance spectroscopy will give us a better understanding of the changes after injury of the cervical spinal cord, brainstem and brain. Correlating the imaging data with the neurological and clinical status of patients could improve the patient status prediction and therapy planning. This study is divided into three sub-projects: i) Reproducibility study of the MR measurements in healthy controls ii) Progression of MR biomarkers in subacute patients with SCI and comparison to chronic patients with SCI iii) Prediction of clinical outcome based on MR biomarkers

Study Type

OBSERVATIONAL

Enrollment

Conditions

Spinal Cord Injuries

Interventions

Healthy controlsOTHER

individuals without spinal cord injury

Subacute SCI patientsOTHER

individuals with spinal cord injury ≥ 2 weeks

Chronic SCI patientsOTHER

individuals with spinal cord injury ≥ 24 months

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 YearsHealthy volunteers:

Medical Language ↔ Plain English

Healthy controls: Inclusion Criteria: * age between 18 and 80 years * no previous history of severe cervical trauma, traumatic brain injury, cervical surgery or signs of neurological impairment and no known neurological disease. Exclusion Criteria: * not meeting the MRI screening requirements * unable to give consent * unable to fulfill the above mentioned inclusion criteria Subacute and chronic patients with spinal cord injury: Inclusion Criteria: * lesion level at or below C3 * etiology of the spinal cord injury is traumatic or non-traumatic * age between 18 and 80 years * time of trauma or onset of symptoms for subacute SCI patients is more than 3 weeks and for the chronic SCI patients more than 2 years Exclusion Criteria: * lesion level below L2 * other known pathology of the spinal cord/brain (e.g. MS) or progressive neurological disorders * inability to meet the MRI screening requirements (e.g. pacemaker or other electronic devices), * severe head trauma as defined by a Glasgow Coma Scale (GCS) of \< 14 * patients who are ventilator dependant

Locations (1)

Swiss Paraplegic Centre

Nottwil, Switzerland

Outcomes

Primary Outcomes

Change in Fractional Anisotropy (FA)

Degree of anisotropy of a diffusion process (value between zero and one). A value of zero means that diffusion is isotropic, i.e. it is unrestricted (or equally restricted) in all directions. A value of one means that diffusion occurs only along one axis and is fully restricted along all other directions. FA is a measure often used in diffusion imaging where it is thought to reflect fiber density, axonal diameter, and myelination in white matter.

Time frame: 16-40 days after injury, 70-96 days after injury, 150- 186 days after injury

Secondary Outcomes

Change in Apparent Diffusion Coefficient (ADC)

Measurement of the magnitude of diffusion (of water molecules) within tissue

Time frame: 16-40 days after injury, 70-96 days after injury, 150- 186 days after injury

Change in Relative Anisotropy (RA)

Measurement of the relative diffusion (of water molecules) within tissue

Time frame: 16-40 days after injury, 70-96 days after injury, 150- 186 days after injury

Data from ClinicalTrials.gov

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