Status:

COMPLETED

EXPLORER PET/CT: Evaluation of Healthy Individuals From Racial/Ethnic Minority Populations

Lead Sponsor:

University of California, Davis

Conditions:

Healthy Volunteers From Racial/Ethnic Minority Populations

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The objective of this pilot study is to collect preliminary data using total body scans on a new, first of its kind, FDA 510k-cleared positron emission tomography/computed tomography (PET/CT) scanner,...

Detailed Description

The aim of this pilot study is to increase the number of healthy individuals from racial/ethnic minority populations. This will advance research being conducted at EMIC by providing "controls" or comp...

Eligibility Criteria

Inclusion

  • Inclusion criteria:
  • Men and women, 18 years of age or older
  • Member of a Federally recognized racial/ethnic minority population, e.g., African American or Black; Hispanic or Latino; Asian American; Native Hawaiian or Other Pacific Islander; Native American or Alaska Native
  • Willing and able to fast for at least 6 hours before and for the duration of the scan
  • Willing to provide urine samples throughout scan visit
  • Willing to provide blood samples for ancestry analysis
  • Willing and able to lay motionless in a supine position for up to 60 minutes and for up to 20 minutes at two separate timepoints
  • Willing and able to give informed consent, personal contact information (phone number, email and postal address), insurance information, and primary care physician contact
  • Exclusion criteria:
  • No Primary Care Physician
  • No health insurance
  • Body weight more than 240 kg (529 pounds)
  • Any known concomitant acute infection (including upper respiratory infection, genitourinary infections, etc.)
  • History of metastatic or newly (last 5 years) diagnosed locally invasive cancer
  • Chemotherapy in the last 5 years
  • Radiation therapy in the last 3 years
  • Major surgery within the last 6 months
  • Pregnancy or breast-feeding
  • Diabetes
  • Fasting blood glucose level \> 200 mg/dL before administration of fluorodeoxyglucose (FDG)
  • Prisoners
  • Self-reported history of dysphoria or anxiety in closed spaces

Exclusion

    Key Trial Info

    Start Date :

    August 18 2021

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    November 8 2021

    Estimated Enrollment :

    20 Patients enrolled

    Trial Details

    Trial ID

    NCT04812080

    Start Date

    August 18 2021

    End Date

    November 8 2021

    Last Update

    April 7 2023

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    University of California, Davis

    Sacramento, California, United States, 95817