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Clinical Trials/NCT06725706
NCT06725706RecruitingNot Applicable

Beta Amyloid PET/CT in Various Aβ-Related Disease

Tianjin Medical University7 sites in 1 country500 target enrollmentStarted: September 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
500
Locations
7
Primary Endpoint
Standardized uptake value (SUV)

Study Overview

Brief Summary

To evaluate the potential usefulness of 18F-92/AV45, 11C-PIB positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various Tau-related disease patients.

Detailed Description

Subjects with various Tau-related disease patients underwent 18F-92/AV45, 11C-PIB PET/CT either for an initial assessment or for recurrence detection. Lesions uptake was quantified by the maximum standard uptake value (SUVmax). The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy of 18F-92/AV45, 11C-PIB PET/CT were calculated.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • - (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 Aβ 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.

Exclusion Criteria

  • - (i) 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.

Arms & Interventions

Single Group Assignment

Each subject receive a single intravenous injection of 18F-92/AV45, 11C-PIB and undergo PET/CT or MRI imaging within the specificed time.

Intervention: 18F-92/AV45, 11C-PIB (Diagnostic Test)

Outcomes

Primary Outcomes

Standardized uptake value (SUV)

Time Frame: 30 days

Standardized uptake value (SUV) of 18F-92/AV45, 11C-PIB for each target lesion of subject or suspected primary tumor or/and metastasis.

Secondary Outcomes

  • Diagnostic efficacy(30 days)

Investigators

Sponsor
Tianjin Medical University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Shaobo Yao, PhD

Prof.

Tianjin Medical University

Study Sites (7)

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