Actively Recruiting

Age: 18Years - 75Years
All Genders
Healthy Volunteers
NCT06043518

CNS Changes Following Upper Limb Loss

Led by University of Zurich · Updated on 2025-11-19

70

Participants Needed

1

Research Sites

208 weeks

Total Duration

On this page

Sponsors

U

University of Zurich

Lead Sponsor

E

ETH Zurich

Collaborating Sponsor

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 congenital upper limb loss. The focus is on the brain's sensory processing and how neuronal changes may relate to clinical measures. By doing so, the hope is to gain insight into the contribution of critical periods to the plasticity of the sensorimotor processing stream. Both macroscopic and microscopic changes of the brain will be examined in individuals with upper limb amelia and compared to healthy controls. fMRI will be combined with behavioural testing to understand which clinical and behavioural determinants drive somatosensory representations along the entire somatosensory processing stream. Using advanced imaging techniques, the aim is to investigate the contribution of brainstem reorganisation to plasticity observed at the cortical level and, by doing so, gain a better understanding of the mechanistic underpinnings of functional reorganisation. Overall, the hope is to provide the first mechanistic insight into whether early life experiences are crucial for the development of the relay nuclei in the central nervous system and how these changes relate to clinical measures such as adaptive behaviours or pain.

CONDITIONS

Official Title

CNS Changes Following Upper Limb Loss

Who Can Participate

Age: 18Years - 75Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 75 years
  • Upper-limb congenital amputees with complete absence of a hand
  • Signed informed consent
  • Healthy subjects aged 18 to 75 years
  • Signed informed consent for healthy subjects
Not Eligible

You will not qualify if you...

  • Contraindications to magnetic resonance imaging
  • Neurological impairment of body function not caused by spinal cord injury
  • Body mass index (BMI) greater than 40
  • Pregnancy
  • Claustrophobia
  • Neurological illness for healthy subjects
  • Impairment of body function induced by a congenital upper-limb amputation (healthy subjects)

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Balgrist Campus

Zurich, Canton of Zurich, Switzerland, 8008

Actively Recruiting

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Research Team

P

Paige Howell, PhD

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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