About this trial
The objective of the study is to construct a noninvasive approach ACP3 targeted PET/CT to detect tumor lesions in patients with prostate cancer and to compare with PSMA/FDG PET/CT.
Eligibility criteria
Qualifiers
Adult patients (aged 18 years or older);
Patients with newly diagnosed, highly suspected recurrence or previously treated metastases of prostate cancer (supporting evidence may include MRI, CT, tumor markers, and pathology report);
Patients who had scheduled both standard-of-care imaging (PSMA/FDG PET/CT) and ACP3 PET/CT scans;
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.
Disqualifiers
The inability or unwillingness of the research participant or legal representative to provide written informed consent.
Trial design
Treatments tested in this trial
- standard-of-care imaging (PSMA/FDG PET/CT), ACP3 PET/CT