Preclinical and preliminary clinical evaluation of [18F]Florbetazine for non-invasive PET detection of cardiac amyloidosis.
Yuying Li, Meijie Pan, Haonan Yu...
https://pubmed.ncbi.nlm.nih.gov/41518400Actively Recruiting
Led by Tianjin Medical University · Updated on 2025-06-04
500
Participants Needed
3
Research Sites
N/A
Total Duration
T
Tianjin Medical University
Lead Sponsor
T
Tianjin Medical University General Hospital
Collaborating Sponsor
Researchers are evaluating the usefulness of a diagnostic imaging test called 18F-92/AV45, 11C-PIB positron emission tomography/computed tomography (PET/CT) in patients with various Tau-related diseases, including primary and metastatic lesions. This study aims to better understand how well this PET/CT scan can detect amyloid-related disease lesions, which are linked to neurodegenerative conditions. The trial is observational and includes adult patients with suspected or diagnosed malignant tumors related to amyloid diseases. Participants will receive a single intravenous injection of the 18F-92/AV45, 11C-PIB tracer. After the injection, they will undergo a PET/CT or MRI scan within a specified time frame to assess the presence of lesions. The uptake of the tracer in lesions will be measured using a standardized uptake value (SUVmax), which helps quantify how much tracer is absorbed by the lesions. During the study, researchers will analyze the imaging results to determine the test's sensitivity, specificity, positive and negative predictive values, and overall accuracy in detecting lesions. Participants will be monitored for about 30 days, during which the standardized uptake value and diagnostic effectiveness will be the primary outcomes measured. The study includes adults aged 18 to 80 years and allows healthy volunteers to participate. Consent and assent are required according to ethical guidelines.
CONDITIONS
Beta Amyloid PET/CT in Various Aβ-Related Disease
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants receive a single intravenous injection of 18F-92/AV45, 11C-PIB and undergo PET/CT or MRI imaging for initial assessment or recurrence detection.
1 visit (in-person)
Duration - 30 days
Participants are observed for diagnostic outcomes and lesion uptake quantification over 30 days following imaging.
Follow-up assessments may occur within this period
Total: 3 locations
1
The First Affiliated Hospital of University of Science and Technology of China
Hefei, Anhui, China, 230000
Actively Recruiting
2
Chinese PLA General Hospital,
Beijing, Beijing Municipality, China, 100853
Actively Recruiting
3
Tianjin Medical University General Hospital
Tianjin, Tianjin Municipality, China, 300052
Actively Recruiting
Y
Ying Wang, MD
L
Li Cai, MD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Yuying Li, Meijie Pan, Haonan Yu...
https://pubmed.ncbi.nlm.nih.gov/41518400