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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03746366
Other study ID # PRO18080481
Secondary ID R01AA025247
Status Completed
Phase Early Phase 1
First received
Last updated
Start date December 1, 2018
Est. completion date July 1, 2020

Study information

Verified date July 2020
Source University of Pittsburgh
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To determine whether alcoholics (AUD) have a greater rate of amyloid positivity (ABeta+) compared to an age-matched cognitively normal control group (HC).


Description:

There is a long-established relationship between alcohol use disorders (AUD), cognitive impairments, and the development of dementia. Some, but not all basic data suggest that alcohol abuse can alter the expression of amyloid precursor protein, and the enzymes that process it. Thus, there is a need for in vivo PET studies to further investigate the relationship between AUD and AD and the mechanism through which alcohol abuse exerts its effect on this type of dementia. Here, we propose to use the amyloid Beta (ABeta) radiotracer carbon-11 labeled Pittsburgh Compound-B ([C-11]PiB) and PET (Klunk et al., 2004) to determine whether AUD increase the risk to be brain ABeta+ in middle aged adults.


Recruitment information / eligibility

Status Completed
Enrollment 39
Est. completion date July 1, 2020
Est. primary completion date July 1, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 65 Years
Eligibility [A] Alcohol Use Disorder Subjects (AUD)

Inclusion Criteria:

1. Males or females between 40 and 65 years old

2. Fulfill DSM-5 criteria for alcohol use disorder of at least moderate severity

3. Current heavy drinking as defined in SAMHSA criteria (i.e., drinking 5 or more drinks on the same occasion on each of 5 or more days in the past 30 days)

Exclusion Criteria:

1. DSM-5 schizophrenia, schizoaffective disorder, bipolar disorder (SCID-5) and prior history of developmental disorders, such as Autism, Down's Syndrome, Intellectual disability.

2. A positive urine drug screen at screening for amphetamines, cocaine, methamphetamine, opioids, barbituates and PCP

3. History of severe unstable medical or neurological illnesses that could affect neuropsychological testing

4. History of cancer (other than skin or in situ prostate cancer) within the previous 5 years

5. Currently pregnant or breastfeeding

6. Currently employed as radiation worker; or participation in radioactive drug research protocols within the previous year

7. Metal implants or paramagnetic objects contained within the body which may interfere with the MRI scan

8. No first-degree relative with Alzheimer's disease or related dementias

(B) Healthy Control Subjects (HC)

Inclusion Criteria:

(1) Males or females between 40 and 65 years old

Exclusion criteria:

1. Current or past DSM-5 psychiatric and/or addictive disorders

2. Current heavy drinking as defined in SAMHSA criteria

3. History of severe unstable medical or neurological illnesses that could affect neuropsychological testing

4. History of cancer (other than skin or in situ prostate cancer) within the previous 5 years

5. Currently pregnant or breastfeeding

6. Currently employed as radiation worker; or participation in radioactive drug research protocols within the previous year

7. Metal implants or paramagnetic objects contained within the body which may interfere with the MRI scan

8. No first-degree relative with Alzheimer's disease or related dementias

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
[C-11]
Radiolabel
Drug:
Pittsburgh Compound B
Tracer

Locations

Country Name City State
United States University of Pittsbyurgh PET Facility Pittsburgh Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
University of Pittsburgh National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary [C-11]PIB + positive/negative Baseline
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