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ENROLLING BY INVITATION
NCT05160480

A Pilot Study of Total-body PET Using FDA-approved Radiotracers Beyond 18F-FDG

Sponsor: University of California, Davis

View on ClinicalTrials.gov

Summary

The purpose of this research study is to test new ways to improve the usefulness of the world's first total-body positron emission tomography (PET)/computed tomography (CT) scanner (EXPLORER) by collecting data from PET scans using one of three different imaging agents: 18F-PSMA; 18F-FES; or, 68Ga DOTATATE. These imaging agents are approved by the FDA to be used for patients diagnosed with prostate cancer (18F-PSMA), neuroendocrine tumor (68Ga DOTATATE), or breast cancer (18F-FES).

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

9

Start Date

2024-06-07

Completion Date

2026-09-01

Last Updated

2026-03-10

Healthy Volunteers

No

Interventions

DIAGNOSTIC_TEST

Total-body PET imaging

Total-body PET imaging at different timepoints

Locations (1)

UC Davis EXPLORER Molecular Imaging Center

Sacramento, California, United States