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Observational Studies             Treatment Trials

Functional magnetic resonance imaging of autonomic physiology in frontotemporal dementia (FTD) and Alzheimer's disease (AD)

Study Director William W. Seeley, MD (PI: Bruce Miller, MD)
Sponsor NIH and Larry L. Hillblom
Recruiting? Yes
Official Study Title Anterior Cingulate, Insular and Frontoinsular Vulnerability in FTLD and AD
Conditions Studied FTD, AD and other closely related neurological disorders including CBD, PSP, and ALS with dementia.
Purpose The purpose of this study is to examine how brain activity relates to autonomic responses in healthy subjects and patients with FTD, AD and other closely related nuerodegenerative diseases.
Eligibility  
Inclusion Criteria Subjects must be enrolled in either the FTD study or ADRC study. Subjects must meet criteria for one of the neurodegenerative diseases mentioned above, unless participating as a control. Subjects must also have an MMSE score above 15.
Exclusion Criteria

Past or current history of alcohol abuse, substance abuse, head trauma (with loss of consciousness greater than 15 minutes), intraparenchymal brain tumor, multiple sclerosis, epilepsy, parkinsonism, hydrocephalus, intracerebral hemorrhage, schizophrenia, or bipolar disorder. Corticol more than four lacunar strokes, intraparenchymal structural lesion or prominent periventricular white matter disease.

Current history of pacemaker, ferromagnetic matter in body, respiratory failure (oxygen-dependent), unipolar depression, anxiety disorder and claustrophobia also exclude subjects from participating

What is Involved?  
Testing FMRI and physiological measurements take approximately 45-60 minutes.
Frequency of Visits 1 visit
Contact Information  
Coordinator Rich Crawford
Phone (415) 476-2941
Materials Needed Prior to Evaluation None
Costs No costs will be charged for any of the study proceedures. Parking will be validated for Millberry Parking Garage for study visit.

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