Actively Recruiting

Age: 18Years - 80Years
All Genders
Healthy Volunteers
ID06725706

Beta Amyloid PET/CT in Various Amyloid-Related Diseases

Led by Tianjin Medical University · Updated on 2025-06-04

500

Participants Needed

3

Research Sites

N/A

Total Duration

On this page

Sponsors

T

Tianjin Medical University

Lead Sponsor

T

Tianjin Medical University General Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Brief Title

Beta Amyloid PET/CT in Various Aβ-Related Disease

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients aged 18 years or older
  • Patients with suspected, newly diagnosed, or previously treated malignant tumors supported by MRI, CT, tumor markers, or pathology
  • Patients scheduled for Beta Amyloid PET/CT scan
  • Able to provide informed consent and assent as per ethics guidelines
Not Eligible

You will not qualify if you...

  • Patients with non-malignant lesions
  • Pregnant patients
  • Unable or unwilling to provide written informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

Trial Site Locations

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

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Research Team

Y

Ying Wang, MD

L

Li Cai, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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