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Clinical Trials/NCT04525612
NCT04525612
Unknown
Early Phase 1

68Ga-BNU-PSMA PET/CT in Patients With Various Types of Cancer

First Affiliated Hospital of Fujian Medical University1 site in 1 country100 target enrollmentAugust 21, 2020

Overview

Phase
Early Phase 1
Intervention
Not specified
Conditions
Tumor
Sponsor
First Affiliated Hospital of Fujian Medical University
Enrollment
100
Locations
1
Primary Endpoint
Standardized uptake value (SUV)
Last Updated
5 years ago

Overview

Brief Summary

To evaluate the potential usefulness of 68Ga-BNU-PSMA positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various types of cancer.

Detailed Description

Subjects with various types of cancer underwent 68Ga-BNU-PSMA PET/CT either for an initial assessment or for recurrence detection. Tumor uptake was quantified by the maximum standard uptake value (SUVmax). The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy of 68Ga-BNU-PSMA PET/CT were calculated.

Registry
clinicaltrials.gov
Start Date
August 21, 2020
End Date
December 30, 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Weibing Miao, PhD

Director, Department of Nuclear Medicine

First Affiliated Hospital of Fujian Medical University

Eligibility Criteria

Inclusion Criteria

  • (i) adult population (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 68Ga-BNU-PSMA 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; (v) healthy volunteers(aged 18 years or order).

Exclusion Criteria

  • (i) patients with pregnancy; (ii) the inability or unwillingness of the research participant, parent or legal representative to provide written informed consent.

Outcomes

Primary Outcomes

Standardized uptake value (SUV)

Time Frame: 30 days

Standardized uptake value (SUV) of 68Ga-BNU-PSMA for each target lesion of subject or suspected primary tumor or/and metastasis.

Secondary Outcomes

  • Diagnostic efficacy(30 days)

Study Sites (1)

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