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CNS Changes Following SCI

Functional, Structural, and Metabolic Central Nervous System Changes Following Damage of the Central Nervous System

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03772548
Enrollment
450
Registered
2018-12-11
Start date
2018-07-18
Completion date
2027-06-30
Last updated
2025-12-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spinal Cord Injuries

Brief summary

The objective of this study is to better understand the structural and functional changes that the central nervous system (CNS) undergoes following spinal cord injury and how these changes relate to clinical measures. Both macroscopic and microscopic changes of the brain and the spinal cord will be examined in SCI patients and compared to healthy controls. In terms of structural plasticity, we aim to identify MR biomarkers that allow predicting the course of the patient's neurological status and accurately describe the course of the disease and the recovery. Importantly, we aim to investigate which factors scale the patients' symptoms. In terms of functional plasticity, we will combine fMRI with behavioural testing to understand which clinical and behavioural determinants drive functional hand representations in the primary somatosensory and motor cortices to be maintained and which determinants drive reorganisation of functional representations following sensory input loss. We will further investigate the contribution of brainstem reorganisation to plasticity observed at the cortical level and, by doing so, aim to better understand the mechanistic underpinnings of functional reorganisation.

Interventions

DIAGNOSTIC_TESTMRI

We will examine acute (\<4 weeks post SCI) to chronic (\>6 months post SCI) patients using functional, structural, and metabolic MRI in both the brain and the spinal cord.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

- Patients: * Age 18-75 * Traumatic or non-traumatic spinal cord injury (para- and tetraplegia) * Acute (\<4 weeks post SCI) to chronic SCI (\> 6 months post SCI) * Signed informed consent

Exclusion criteria

- Patients: * Contraindications to magnetic resonance imaging * Neurological impairment of body function impairments not induced by spinal cord injury * BMI \> 40 * Pregnancy * Claustrophobia Inclusion Criteria - Healthy subjects: * Age 18-75 * Signed Informed consent

Design outcomes

Primary

MeasureTime frameDescription
Conventional magnetic resonance imaging (MRI) parameterUp to 50 weeksStructural characteristics in the brain and cervical spinal cord are assessed in acute to chronic spinal cord injury (SCI) patients using conventional MRI and compared to healthy controls

Secondary

MeasureTime frameDescription
Magnetic resonance spectroscopy (MRS) parameterUp to 50 weeksMetabolic parameters are assessed in acute to chronic SCI patients using MRS in the brain and cervical spinal cord and compared to healthy controls
Change of functional MRI (fMRI) parameter between 2 to 4 time pointsUp to 50 weeksChange of brain activities is assessed between 2 to 4 time points using fMRI during resting-state or a specific task in acute to chronic SCI patients and compared to healthy controls

Countries

Switzerland

Contacts

Primary ContactMaryam Seif, PD Dr.
maryam.seif@balgrist.ch+41 44 510 72 14
Backup ContactSanne Kikkert
sanne.kikkert@balgrist.ch+41 44 633 27 15

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026