Lung Cancer Clinical Trial

Comparison of Imaging Characteristics of uEXPLORER and Conventional PET/CT in Patients With Lung Cancer, Lymphoma, and Melanoma

Summary

To determine the minimum scan duration for fluorine-18 positron-emitting radioactive isotope-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET)/computed tomography (CT) scans performed on a total-body PET/CT scanner that results in non-inferior image quality to 18F-FDG PET/CT scans performed on a conventional PET/CT scanner. The subject population will be patients being staged for lung cancer, lymphoma, or melanoma.

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Eligibility Criteria

Inclusion Criteria:

Ability to understand and willingness to sign an informed consent form.
Ability to adhere to the study visit schedule and all protocol requirements.
Men and women ≥18 years of age.
Diagnosis or suspected diagnosis of lung cancer, melanoma or lymphoma.
Patients who have been referred for a PET/CT scan.

Exclusion Criteria:

Pregnant women.
Claustrophobia.
Any significant medical condition that in the opinion of the investigator would prevent the subject from participating and/or adhering to study related procedures or interfere with subject safety.

Study is for people with:

Lung Cancer

Estimated Enrollment:

180

Study ID:

NCT04478318

Recruitment Status:

Enrolling by invitation

Sponsor:

University of California, Davis

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There is 1 Location for this study

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University of California Davis
Sacramento California, 95817, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Estimated Enrollment:

180

Study ID:

NCT04478318

Recruitment Status:

Enrolling by invitation

Sponsor:


University of California, Davis

How clear is this clinincal trial information?

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