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A Magnetic Resonance Imaging Study of Patients With Cervical Spondylosis

Structural Spinal Cord Integrity in Patients With Cervical Spondylosis in Relation to Clinical Status

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01243684
Acronym
Tractocervical
Enrollment
40
Registered
2010-11-18
Start date
2010-09-01
Completion date
2014-01-01
Last updated
2026-02-13

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

Conditions

Cervical Spondylosis

Keywords

Spinal cord, cervical spondylosis, myelopathy

Brief summary

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

Detailed 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.

Interventions

DEVICEDTI - Diffusor Tensor Imaging

Radiology intervention

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
DTI parameters in cervical spinal cord3 weeks

Secondary

MeasureTime frameDescription
Clinical data, i.e., Muscle testing, sensory testing, reflexes, spasticity, and Motor function (dexterity test), grip strength3 weeksClinical data, i.e., Muscle testing, sensory testing, reflexes, spasticity Motor function (dexterity test), grip strength

Countries

France

Contacts

PRINCIPAL_INVESTIGATORAntoine FEYDY, PhD

Assistance Publique Hopitaux de Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 14, 2026