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Tractography and Diffusion Tensor Imaging of the Human Spinal Cord in Healthy Subjects : Anatomical Atlas

Tractography and Diffusion Tensor Imaging of the Human Spinal Cord in Healthy Subjects : Anatomical Atlas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05079945
Acronym
TRACTOCORD
Enrollment
49
Registered
2021-10-15
Start date
2022-02-05
Completion date
2022-04-30
Last updated
2025-09-03

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

Conditions

Healthy Volunteer

Keywords

Tractography, DTI, MRI, spinal cord

Brief summary

Today, Spinal cord pathologies, whether are tumoral, vascular, traumatic, malformative, inflammatory, or degenerative still constitute a major medico-surgical challenge due to the particular anatomy of the spinal cord. Indeed, the spinal fibers (whether they have a sensory or motor function) are all condensed in an extremely small volume. To date, there is no reliable technique to know the precise position of the spinal tracts specifically involved in the sensory and motor functions of the upper and lower limbs. The purpose of this study is to evaluate the feasibility for differentiating spinal tracts by tractography from a cerebral Diffusion tensor imaging (DTI) Magnetic Resonance Imaging (MRI) sequence (associated with an anatomical sequence) by performing a stitching process with spinal cord DTI MRI sequence, in healthy subjects. The criterion of differentiation of the tracts will be assessed by highlighting already known cerebral tracts (cortico-spinal fibers, spinothalamic, posterior cord) and which will be monitored at the spinal level.

Interventions

PROCEDURESpinal cord Tractography in order to differentiate spinal tracts.

Spinal cord tractography using DTI MRI sequences of the brain and spinal cord, in order to differentiate tracts at the spinal cord level; and by performing a stitching process between Brain and Spinal cord DTI sequences.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

* patient\> 18 years old * Healthy volunteer * Social insured in France * Patient who signed the informed consent of the study

Exclusion criteria

* Medical or surgical history of disease that may affect the central nervous system, or the spine * History of spine or spinal cord trauma. * Spinal osteoarthritis which can lead to a medullary hyper signal. * Contraindication to MRI: claustrophobia, pace-maker, defibrillator, metallic foreign bodies, etc. * Subjects benefiting from legal protection (curatorship, guardianship or safeguard of justice). * Pregnant and / or breastfeeding woman.

Design outcomes

Primary

MeasureTime frameDescription
Spinal tracts differentiation and identificationdate of Tractography procedure (DTI MRI)Percentage of complete tracts identified among healthy volunteer

Secondary

MeasureTime frameDescription
Spinal cord Tracts Atlas12 months (end of recruitment and exams)Elaboration of a tracts classification using a algorithm based on the type, the volume and the fraction of anisotropy and mean diffusivity of each tract

Countries

France

Outcome results

None listed

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