UAB Alzheimer's Disease Center Core Cohort - Imaging Substudy



Status:Recruiting
Conditions:Alzheimer Disease
Therapuetic Areas:Neurology
Healthy:No
Age Range:50 - Any
Updated:4/26/2018
Start Date:April 20, 2018
End Date:April 1, 2024
Contact:April Riddle
Email:ariddle@uabmc.edu
Phone:2059346504

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The primary objective of this study is to measure the concentration and the regional brain
distribution of pathologic amyloid deposition using the PET tracer [C-11]PiB in participants
in the UAB Alzheimer's Disease Center cohort. Assessment of interactions between race and
vascular risk factors, brain amyloid levels measured with [C-11]PiB-PET, and cognitive status
will be the primary outcome of this imaging study.

The primary objective of this study is to measure the concentration and the regional brain
distribution of pathologic amyloid deposition using the PET tracer [C-11]PiB in participants
in the UAB-ADC cohort. The amount and distribution of [C-11]PiB in the brain will be
correlated to demographic, clinical, genetic, and biospecimen data acquired through the
separate ongoing UAB-ADC study. Assessment of interactions between race and vascular risk
factors, brain amyloid levels measured with [C-11]PiB-PET, and cognitive status will be the
primary outcome of this imaging study. As a secondary aim, the investigators will assess the
ability of the early flow frames from [C-11]PiB-PET and brain volumetric measurements with
MRI to serve as a marker of neuronal injury and to predict cognitive status in conjunction
with the amyloid-PET results.

Inclusion Criteria:

- 1. Enrollment in the UAB-ADC study under a separate IRB-approved research protocol
(IRB-300000169).

2. Negative urine or serum B-hCG test within 2 days of [C-11]PiB administration in women of
child bearing potential. Women who are post-menopausal with at least 1 year since last
menses or documented surgical sterilization will not require pregnancy testing.

Exclusion Criteria:

1. Meets any exclusion criteria for the UAB-ADC study (IRB-300000169).

2. Inability or contraindication for undergoing MRI and/or PET imaging

3. Inability to participate in the imaging studies due to severity of dementia
We found this trial at
1
site
Birmingham, Alabama 35233
Principal Investigator: Jonathan McConathy, MD, PhD
Phone: 205-996-7115
?
mi
from
Birmingham, AL
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