Study to Evaluate the Relative Bioavailability of a New Formulation of NPT 2042 Soft-Gelatin Capsules Compared to the Original Formulation of NPT 2042
NCT07222878
Alzheimer Disease, Brain Diseases
Lincoln, Nebraska, United States
View Trial DetailsNCT Number: NCT04436341
In the current study, the investigators will examine the extent of subclinical epileptic activity in patients with Alzheimer's disease and patients with Lewy body dementia as compared to healthy elderly controls. The participants will wear a new device called "ear-EEG", which makes it possible to record EEG for longer periods of time while at home. Furthermore, the investigators want to investigate whether there is an association between subclinical epileptic activity and the cerebral blood flow as measured with functional MRI.
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Notify Me50 year–90 year
All sexes
Observational
Gunhild Waldemar, Copenhagen, Copenhagen OE, Denmark
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(Alzheimer's disease):
Exclusion criteria
(Alzheimer's disease):
Inclusion criteria
(Lewy body dementia):
Exclusion criteria
(Lewy body dementia):
Inclusion criteria
(Healthy controls):
Exclusion criteria
(Healthy controls):
Time frame: 8 months
If it is possible for patients with Alzheimer's disease to wear ear-EEG for at least 24 hours including 5 hours of sleep during a 48 hours period
Time frame: 2 years
Compare the prevalence and type of paroxysmal activity as measured with the ear-EEG in patients with Alzheimer's disease and Lewy body dementia as compared to healthy elderly controls
Time frame: 2 years
Compare the amount of paroxysmal activity as measured with ear-EEG and the cerebral blood flow (rCBF) as measured with arterial spin labeling fMRI in patients with Alzheimer's disease and Lewy body dementia
Danish Dementia Research Centre
Network
Acronym: AD-LBD-EPI
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