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Clinical Trials/NCT04982458
NCT04982458
Unknown
Not Applicable

Clinical Study of 68 GA-FAPI PET Imaging Noninvasive Visible Fibrosis Formation in Heart Failure

Wuhan Union Hospital, China1 site in 1 country50 target enrollmentAugust 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
Wuhan Union Hospital, China
Enrollment
50
Locations
1
Primary Endpoint
Sensitivity and specificity of 68Ga-FAPI PET for diagnosis and staging in heart failure.
Last Updated
3 years ago

Overview

Brief Summary

This is a diagnostic study. Patients were included from patients with clinically suspected or confirmed heart failure, and 68Ga-FAPI and 13N-NH3 gated myocardial imaging were performed to evaluate the effectiveness of 68Ga-FAPI PET imaging in visualizing the degree of myocardial fibrosis in patients with heart failure. The subjects completed 68Ga-FAPI and 13N-NH3 gated myocardial imaging in a one-stop process, and collected general information, clinical data, echocardiography, blood routine, liver and kidney function indicators, 68Ga-FAPI and 13N-NH3 PET imaging results and other imaging data of the patients and volunteers.

Detailed Description

Fibroblast activated protein (FAP) is a type II membrane-bound glycoprotein that is highly specifically expressed in activated fibroblast reactions. The 68Ga labeled fibroblast activated protein inhibitor (68 ga-fapi) has shown advantages of high uptake and high image contrast in imaging the activated fibroblast response, including its successful use in visualizing the degree of liver fibrosis. The molecular imaging probe targeting FAP combined with the mature myocardial perfusion imaging agent 13N-NH3 can help us to achieve the following objectives: On the one hand, to investigate the myocardial fibrosis in patients with heart failure and to visualize the formation of fiBER-activated protein in the process of heart failure; At the same time, the performance of 68GA-FAPI in differential diagnosis of heart failure and grading of heart failure degree was discussed, so as to make up for the insufficiency of clinical routine imaging technology in the diagnosis of myocardial fibrosis in heart failure.

Registry
clinicaltrials.gov
Start Date
August 1, 2021
End Date
December 31, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Wuhan Union Hospital, China
Responsible Party
Principal Investigator
Principal Investigator

Xiaoli Lan

Director of the Department of nuclear medicine

Wuhan Union Hospital, China

Eligibility Criteria

Inclusion Criteria

  • Adult patients (age 18 years or above), gender is not limited;
  • Patients with clinically suspected or confirmed heart failure (supporting evidence includes visual examination, cardiac MRI, cardiac ultrasound, and serological indicators, etc.), and patients who agree to undergo 68Ga-FAPI and 13N-NH3 imaging;
  • The patient or his legal representative can sign the informed consent.

Exclusion Criteria

  • Acute systemic diseases and electrolyte disorders;
  • Pregnant or lactating women;
  • Patients refuse to sign the informed consent.

Outcomes

Primary Outcomes

Sensitivity and specificity of 68Ga-FAPI PET for diagnosis and staging in heart failure.

Time Frame: 2 years

For 50 subjects with suspected or diagnosed or treated heart failure who have completed 13N-NH3 imaging, diagnosis and staging results of 68Ga-FAPI PET will be compared to pathology, clinical and follow-up result.

Study Sites (1)

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