Actively Recruiting

Age: 18Years - 75Years
All Genders
Healthy Volunteers
NCT03772548

CNS Changes Following SCI

Led by University of Zurich · Updated on 2025-12-15

450

Participants Needed

1

Research Sites

467 weeks

Total Duration

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AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

CNS Changes Following SCI

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 to 75 years
  • Traumatic or non-traumatic spinal cord injury causing para- or tetraplegia
  • Acute spinal cord injury less than 4 weeks old to chronic injury more than 6 months old
  • Signed informed consent
  • Healthy subjects aged 18 to 75 years
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Contraindications to magnetic resonance imaging
  • Neurological impairments not caused by spinal cord injury
  • Body mass index (BMI) greater than 40
  • Pregnancy
  • Claustrophobia

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Universitätsklinik Balgrist

Zurich, Switzerland, 8008

Actively Recruiting

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Research Team

M

Maryam Seif, PD Dr.

CONTACT

S

Sanne Kikkert

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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