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Establishment of a calibration sample for the evaluation of MRI perfusion measurement of cerebral blood flow at the individual case level: further development of the imaging-based differential diagnosis of dementia syndromes

Establishment of a calibration sample for the evaluation of MRI perfusion measurement of cerebral blood flow at the individual case level: further development of the imaging-based differential diagnosis of dementia syndromes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033740
Enrollment
180
Registered
2024-03-04
Start date
2024-06-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

The scientific question of the described research programme deals with the improvement of the early diagnosis of neurodegenerative diseases, especially dementia, through the further development and use of multimodal PET/MRI imaging techniques. The main aim of the project is to increase diagnostic accuracy and efficiency in order to enable more valid and reliable identification of patients with incipient memory impairment, particularly in relation to Alzheimers disease.

Interventions

Group 1: Study group: The scientific question of the described research program deals with the improvement of early diagnosis of neurodegenerative diseases, especially dementia, by the further develop

Sponsors

Klinik für Nuklearmedizin, Universitätsklinikum Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age: between 50-80 years Absence of neurological or psychiatric disorders, especially epilepsy, migraine, chronic tension headaches Absence of severe or chronic physical illness Absence of use of psychotropic substances Absence of pregnancy High-grade stenosis of the neck vessels (>70 %)

Exclusion criteria

Exclusion criteria: MRI exclusion criteria: - Hydrocephalus shunt - Metal implants in the head and/or body - Condition after severe craniocerebral trauma or after surgery for brain tumours brain tumours - Pacemaker - Absence of a declaration of consent Exclusion criteria for 18(F)-FDG PET examination: - The blood glucose level is determined before the FDG injection. In case of hyperglycaemia, FDG uptake may be reduced. If the glucose level is above 150-200 mg/dl, the examination cannot be performed or or at a later time after the glucose level has been checked again. - Presence of pregnancy - Because the FDG-PET examination is performed in the magnetic field of the PET /MRI device, all MRI-related exclusion criteria also apply (see exclusion criteria also apply (see above).

Design outcomes

Primary

MeasureTime frame
Correlation between F-18 FDG-PET activity and ASL perfusion

Secondary

MeasureTime frame
Differences between the sexes and the age decades

Countries

Germany

Contacts

Public ContactJoachim Strobel

Klinik für Nuklearmedizin, Universitätsklinikum Ulm

joachim.strobel@uniklinik-ulm.de+49 731 500 61301

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026