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Clinical Trial Summary

This prospective study aims: 1. to compare cognitive performance in different clinical groups of participants with mild cognitive impairment (MCI) or mild dementia [Alzheimer's Disease (AD), Vascular Cognitive Impairment (VCI) and Fronto-temporal Dementia (FTD)] to determine whether scores reveal differential profiles between the groups, 2. to demonstrate differences in imaging markers between different dementia syndromes and healthy volunteers using ultra high-field MRI at 7T.


Clinical Trial Description

The imaging arm of the study include: 1. to demonstrate differences in brain iron levels between different dementia syndromes and healthy volunteers using ultra high-field MRI, quantitative susceptibility mapping (QSM) at 7T. 2. to demonstrate variations in the resting oxygen usage as an important biomarker to discriminate between different dementia syndromes. 3. to demonstrate cerebral blood flow changes in the brain, particularly in the hippocampus region, and its correlation with different dementia syndromes using Arterial Spin Labelling MRI technique. 4. to demonstrate increased blood brain barrier leakage in the brain, particularly in the hippocampus region, and its correlation with Alzheimer's Disease (AD) and Vascular Cognitive Impairment (VCI) using a new dynamic contrast-enhanced MRI (DCE-MRI) technique. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03861884
Study type Observational
Source Nottingham University Hospitals NHS Trust
Contact Akram Dr Hosseini
Phone 0115 924 9924
Email Akram.Hosseini@nuh.nhs.uk
Status Recruiting
Phase
Start date December 12, 2018
Completion date March 2025