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MRI in the fast lane: MR-STAT

MRI in the fast lane: MR-STAT - MR-STAT

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON48176
Enrollment
50
Registered
2019-06-19
Start date
2019-11-11
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Overige zenuwstelsel-aandoeningen: demyeliniserende aandoeningen (MS), neoplasmata en epilepsie Stroke

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a patient must meet the following criteria: • Age >= 18 years • Diagnosed with one of the following neurological diseases: primary brain tumor, epilepsy, MS or ischemic stroke • Previous imaging findings characteristic of particular neurological disease • Ability to lie supine in the MRI scanner for 45 minutesAlthough not an inclusion criterion, care is taken to select those patients that are already scheduled for a standard clinical follow-up MRI examination within the next 4 months, thereby limiting patient burden by providing the option to combine both study- and clinical MRI examination on the same day.Inclusion criteria for healthy volunteers are the following: • Age >= 18 years • No history of neurological diseases

Exclusion criteria

Exclusion criteria: Patients will be excluded when meeting one of the following criteria: • Atypical imaging findings not characteristic for the neurological diagnosisExclusion criteria for the healthy volunteers are as follows: • History of any neurological disease

Design outcomes

Primary

MeasureTime frame
The main study parameter will be the image quality scores of the MR-STAT-generated image data sets with regard to overall image quality, image artifacts, and visualization of several predefined anatomical structures; these scores will be compared with those of the standard MRI data sets.

Secondary

MeasureTime frame
The secondary study parameter will be the image quality of the MR-STAT-generated image data sets compared with the standard MRI data sets, assessed in a side-by-side fashion.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)