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Rotating Frame Relaxation Imaging in Patients With Multiple Sclerosis

Rotating Frame Relaxation Imaging in Patients With Multiple Sclerosis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02403570
Acronym
ROMUS
Enrollment
21
Registered
2015-03-31
Start date
2015-02-28
Completion date
2016-12-31
Last updated
2021-03-03

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

Conditions

Multiple Sclerosis, Multiple Sclerosis, Chronic Progressive, Multiple Sclerosis, Relapsing-Remitting

Keywords

Multiple Sclerosis, MRI, rotating frame

Brief summary

The aim of this study is to develop novel magnetic resonance imaging (MRI) protocols suitable for patients with multiple sclerosis using advanced MRI such as rotating frame relaxation imaging. In addition, the investigators want to study the correlation between advanced MRI parameters and clinical disease progression.

Interventions

OTHERBrain MRI

Sponsors

Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* The diagnosis of relapsing remitting MS made according to the Poser, McDonald's or revised McDonald's criteria (Group I) before participating in the study * Initial MS diagnosis of relapsing remitting form of the disease according to the criteria as mentioned above, and conversion into the secondary progressive phase of the disease as evaluated by the referring neurologist according to the clinical evaluation and confirmed by the study physician (Group II). * Mental status: Patients must be able to understand the meaning of the study * Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff

Exclusion criteria

* Any other autoimmune disease than MS requiring immunomodulatory or immunosuppressive medication * High-dose corticosteroid treatment within 30 days before participating in the study * Prior medical history: Patient must have no history of serious cardiovascular, liver or kidney disease * Any psychiatric condition that compromises the subject's ability to participate in the study * Infections: Patient must not have an uncontrolled serious infection * No contraindications for MRI (cardiac pacemaker, intracranial clips etc)

Design outcomes

Primary

MeasureTime frameDescription
MR relaxation values 0BaselineAim is to measure different quantitative MR relaxation values (e.g. Traff, T1rho) in different brain areas of patients with MS at baseline
MR relaxation values 1One yearAim is to measure different quantitative MR relaxation values (e.g. Traff, T1rho) in different brain areas of patients with MS after one year follow-up

Secondary

MeasureTime frameDescription
MR relaxation values and clinical markers 0BaselineAim is to study the correlation between MR relaxation values and clinical markers of MS at baseline
MR relaxation values and clinical markers 1One yearAim is to study the correlation between MR relaxation values and clinical markers of MS after one year follow up

Countries

Finland

Outcome results

None listed

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