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MR Imaging Biomarker for the Characterization of dynamic metabolic processes in patients with aberrant glucose and/or neurotransmitter metabolism

Conditions
EpilepsyBrain tumors
Registration Number
DRKS00031213
Lead Sponsor
Medizinische Universität Wien
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Brain tumor patients:
(glucose-avid brain lesions: 5 with cerebral metastases, 5 with lymphomas, 10 high-grade gliomas according to the updated WHO classification 2021) with a Karnofsky performance status =70% who received a routine MRI protocol at 3 T including contrast medium -enhancing agents within two weeks prior to the first study-related measurement but before any biopsy, resection, or radiosurgery occurred. For this pilot study, the group of patients with brain metastases will include distant metastases of all types of primary tumors)
Epilepsy patients:
(Clearly defined epileptogenic lesions in MRI such as malformations of cortical development, vascular malformations, scars, etc., routine clinical examinations including long-term video EEG monitoring, FDG-PET, routine clinical T1/T2-weighted MRI)

Exclusion Criteria

MRI inclusion and exclusion criteria:
- Exclusion of pregnancy
- Exclusion of nursing mothers
- Anamnestic exclusion of a metal implantation (pacemaker, metal heart valves, surgical clips, implanted electronic infusion pumps, tattoos and the like).
- Exclusion of a contrast medium allergy
- Anamnestic exclusion of claustrophobia
- Exclude recent head/brain surgery
- Exclusion of a metabolic disorder (HbA1c>6%)

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
It is possible to detect metabolic changes in glucose/neurotransmitter metabolism in selected brain pathologies (e.g. brain tumors, epilepsy) with expected metabolic changes.
Secondary Outcome Measures
NameTimeMethod
on-invasive imaging of glucose and neurotransmitter metabolism via time-resolved MRSI is possible using both clinical routine 3T and experimental 7T MR scanners.
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