About this trial
To evaluate the potential usefulness of 18F-FPyCO/SMBT-1 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various MAO-B-related disease patients.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
None
Disqualifiers
patients with non-malignant lesions; (ii) patients with pregnancy; (iii) the inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.
Trial population
(i) adult patients (aged 18 years or order); (ii) patients with suspected or new diagnosed or previously treated PD (supporting evidence may include MRI, CT, tumor markers and pathology report); (iii) patients who had scheduled MAO-B 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
Diagnostic Test: 18F-FPyCO/SMBT-1
Diagnostic testEach subject receive a single intravenous injection of 18F-FPyCO/SMBT-1, and undergo PET/ CT or MRI imaging within the specificed time.
Treatment groups
Trial outcomes
Primary outcomes
Standardized uptake value (SUV)
Standardized uptake value (SUV) of 18F-FPyCO/SMBT-1 for each target lesion of subject or suspected PD.
Secondary outcomes
Diagnostic efficacy
The sensitivity, specificity and accuracy of MAO-B PET/CT were calculated
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Tianjin Medical University
Lead sponsor
Tianjin Medical University General Hospital
Collaborator