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A Magnetic Resonance Imaging Study of Patients With Cervical Spondylosis (Tractocervical)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Cervical Spondylosis

Treatments

Device: DTI - Diffusor Tensor Imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT01243684
P090404

Details and patient eligibility

About

This study aims at evaluating spinal cord structure using diffusion tensor imaging in patients with cervical spondylosis.

Full description

Diffusion tensor imaging (DTI) of the cervical spinal cord will be performed in patients with cervical spondylosis with varying degrees of symptoms and in healthy control subjects. Fibre tracking of main spinal tracts will be performed. Regions of interest will also be identified. Diffusion parameters will be extracted. This will allow quantification of degree of damage in of the spinal cord. The findings will be related to motor function measures and comprehensive clinical tests of sensory and motor function.

Enrollment

40 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18-70 years old
  • Sufficiently cooperative
  • Cognitively understands study and implications
  • Signed informed consent
  • Symptomatic cervical spondylosis

Exclusion criteria

  • MRI contraindications (e.g., pacemaker, metal implants, claustrophobia)
  • Previous pathology that would impact behavioural measures
  • Anxiety and poor cooperation
  • Previous neurological condition
  • Pregnancy

Trial design

Primary purpose

Diagnostic

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Healty volunteers
Active Comparator group
Treatment:
Device: DTI - Diffusor Tensor Imaging
Patients
Experimental group
Treatment:
Device: DTI - Diffusor Tensor Imaging

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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