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Combined perfusion MRI and MR spectroscopy in multiple sclerosis

Combined perfusion MRI and MR spectroscopy in multiple sclerosis - MRI and MRS in MS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON30006
Enrollment
60
Registered
2006-12-04
Start date
2006-09-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

multiple sclerosis

Interventions

None listed

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusioncriteria patients: - age 18-60 years - diagnosis of multiple sclerosis according to the McDonald-criteria (McDonald et al., 2001). - written informed consent;Inclusioncriteria controls: - age eightteen and older - written informed consent

Exclusion criteria

Exclusion criteria: Exclusioncriteria patients: - use of systemic corticosteroids in the eight weeks before start of the study - use of immunomodulating therapies (interferon-ß, glatiramer acetate) - a history of cerebral pathology other than MS (brain infarct, brain haemorrhage, Parkinson's disease, Alzheimer's disease, cerebral vasculitis, brain absces) - Diabetes mellitus;Exclusiecriteria controls: - a history of cerebral pathology (brain infarct, brain haemorrhage, Parkinson's disease, Alzheimer's disease, cerebral vasculitis, brain absces) - Diabetes mellitus

Design outcomes

Primary

MeasureTime frame
Primary endpoints: - The difference in measures of cerebral perfusion between the groups of RRMS, SPMS, PPMS patients and healthy controls. - The difference in measures of cerebral metabolism (as measured with MR spectroscopy) between the groups of RRMS, SPMS, PPMS patients and healthy controls. - The correlation between measures of cerebral perfusion and cerebral metabolism in the groups RRMS, SPMS, PPMS and healthy control persons.

Secondary

MeasureTime frame
Secondary endpoints: - the correlation between clinical measures of disability with measures of cerebral perfusion - the correlation of clinical measures of disability with measures of cerebral metabolism

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)