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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05076331
Other study ID # 2020-125
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date April 20, 2021
Est. completion date December 30, 2023

Study information

Verified date October 2021
Source University of North Texas Health Science Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this project is to study the aging brain among participants enrolled in the Health and Aging Brain Study: Health Disparities project . There are a number of things that can influence how people think as they age, including diabetes, depression, as well as our biology. In this study, the investigators seek to study the aging brain by using brain PET scans that create detailed pictures of the brain.


Description:

There are a number of things that can influence how we think as people age, including diabetes, depression, as well as our biology. In this study, the investigators are using PET scans with a tracer to create detailed pictures of the brain. This information will be used to help the investigators understand how the brain ages and in the future could be used to develop better diagnostics and treatments for Alzheimer's disease and memory loss in Mexican Americans, African Americans, and non-Hispanic whites. The goal of this study is to address this disparity by enrolling ethnically diverse participants in this study.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 3000
Est. completion date December 30, 2023
Est. primary completion date August 30, 2023
Accepts healthy volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: 1. Enrolled in the Health and Aging Brain Study HD: Health Disparities project 2. Provided consent to re-contact 3. Willing and capable of undergoing PET scan of the head Exclusion Criteria: 1. Inability to provide informed consent by self or by proxy. 2. Pregnant or breast feeding women* 3. History of alcoholism or drug dependency/abuse within the last 2 years before screening 4. Hypersensitivity to the active substance or to any of the following excipients is contraindicated: sodium dihydrogen phosphate, phosphoric acid, sodium ascorbate, ethanol (anhydrous), water for injection 5. Participants may not be in this study if they do not meet the safety criteria to undergo imaging procedures.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
PI-2620 tracer for Tau PET scan
Tau PET scans are obtained using PI-2620 tracer provided by Life Medical Imaging.

Locations

Country Name City State
United States University of North Texas Health Science Center Fort Worth Texas

Sponsors (1)

Lead Sponsor Collaborator
University of North Texas Health Science Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health Disparities in Aging Examine the prevalence of Tau burden among a multi ethnic cohort Through study completion in 2 years
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