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Évaluation de l'Impact du Compressed Sensing Sur le Signal QSM

Évaluation de l'Impact du Compressed Sensing Sur le Signal QSM

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04907487
Acronym
CS-QSM
Enrollment
82
Registered
2021-05-28
Start date
2021-12-15
Completion date
2025-05-14
Last updated
2026-01-05

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

Conditions

MRI

Brief summary

Patients who have agreed to participate in the study will complete the MRI protocol as part of routine care, to which a maximum of four additional 25-minute sequences will be added. MRI of routine care includes at least the following sequences: * 3D T1 TFE (2 minutes) * T2 TSE (2 minutes) * 3D FLAIR (3 minutes) The sequences added by the research lasting 25 minutes are: * SWI QSM 1.0iso 8 echoes (10 minutes) * SWI QSM 1.0iso 8 echoes CS 6 (7 minutes) * SWI QSM 1.0iso 8 echoes CS 9 (5 minutes) * SWI QSM 1.0iso 8 echoes CS 12 (3 minutes)

Detailed description

Patients who have agreed to participate in the study will complete the MRI protocol as part of routine care, to which a maximum of four additional 25-minute sequences will be added. MRI of routine care includes at least the following sequences: * 3D T1 TFE (2 minutes) * T2 TSE (2 minutes) * 3D FLAIR (3 minutes) The sequences added by the research lasting 25 minutes are: * SWI QSM 1.0iso 8 echoes (10 minutes) * SWI QSM 1.0iso 8 echoes CS 6 (7 minutes) * SWI QSM 1.0iso 8 echoes CS 9 (5 minutes) * SWI QSM 1.0iso 8 echoes CS 12 (3 minutes)

Interventions

DEVICEMRI

MRI of routine care includes at least the following sequences: * 3D T1 TFE (2 minutes) * T2 TSE (2 minutes) * 3D FLAIR (3 minutes) The sequences added by the research lasting 25 minutes are: * SWI QSM 1.0iso 8 echoes (10 minutes) * SWI QSM 1.0iso 8 echoes CS 6 (7 minutes) * SWI QSM 1.0iso 8 echoes CS 9 (5 minutes) * SWI QSM 1.0iso 8 echoes CS 12 (3 minutes)

Sponsors

Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For patients with MS: * Patient over 18 years old * Presenting MS defined according to McDonald's revised criteria for spatial and temporal clinical or radiological dissemination \[16\], * Should benefit as part of the care of an MRI examination with or without injection of gadolinium * Express consent to participate in the study * Affiliate or beneficiary of a social security scheme For patients with an indication to undergo a brain MRI and at low risk of inflammatory CNS disease: * Patient over 18 years old * Should benefit as part of the care of an MRI examination with or without injection of gadolinium * Express consent to participate in the study * Affiliate or beneficiary of a social security scheme

Exclusion criteria

* For patients with MS: * Patient benefiting from a legal protection measure * Pregnant or breastfeeding woman For patients with an indication to undergo a brain MRI and at low risk of inflammatory CNS disease: * Patient benefiting from a legal protection measure * Pregnant or breastfeeding woman * Patient with inflammatory and / or demyelinating pathology of the CNS Secondary

Design outcomes

Primary

MeasureTime frameDescription
concordance of QSM signal with and without compressed-sensing in white matter1 DAYconcordance of QSM signal with and without compressed-sensing in white matter

Countries

France

Outcome results

None listed

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