About this trial
To evaluate the potential usefulness of 68Ga/18F-PSMA/PSFA positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various PSMA-related disease patients (prostate cancer, hepatic cancer, etc.).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
None
Trial population
(i) adult patients (aged 18 years or order); (ii) patients with suspected or new diagnosed or previously treated malignant tumors (supporting evidence may include MRI, CT, tumor markers and pathology report); (iii) patients who had scheduled PSMA PET/CT scan; (iv) patients who were able to provide informed consent (signed by participant, parent or legal representative) and assent according to the guidelines of the Clinical Research Ethics Committee.
Trial design
Cohort
Prospective
Treatments tested in this trial
68Ga/18F-PSMA/PSFA
Diagnostic testEach subject receive a single intravenous injection of 68Ga/18F-PSMA/PSFA, and undergo PET/CT imaging within the specificed time.
Treatment groups
Trial outcomes
Primary outcomes
Standardized uptake value (SUV)
Standardized uptake value (SUV) of PSMA for each target lesion of subject or suspected primary tumor or/and metastasis.
Secondary outcomes
Diagnostic efficacy
The sensitivity, specificity and accuracy of PSMA PET/CT were calculated.
Sponsors and contacts
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Tianjin Medical University
Lead sponsor
Tianjin Medical University General Hospital
Collaborator