Actively Recruiting

Age: 18Years +
All Genders
NCT07151521

(68)Ga-FAPI PET/CT in Patients With ANCA-associated Vasculitis

Led by Ruijin Hospital · Updated on 2025-11-17

30

Participants Needed

1

Research Sites

147 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pulmonary and renal involvement are the most common clinical manifestations of antineutrophil cytoplasmic antibody(ANCA)-associated vasculitis (AAV). Studies have shown that both interstitial lung disease (ILD) and renal dysfunction are closely associated with poor prognosis in patients with AAV. Therefore, early identification of whether AAV patients have concomitant ILD and renal involvement is of great clinical importance for assessing disease severity, stratifying prognostic risk, and developing individualized treatment strategies. Positron emission tomography (PET) is a noninvasive molecular imaging technique that can provide decision-making support for early and accurate diagnosis, timely intervention, as well as evaluation of treatment response and prognosis. In the same individual, PET enables whole-body localization of disease in a single examination, overcoming the limitation of conventional diagnostic methods that typically assess only one region at a time, thereby facilitating patient benefit. In recent years, many novel PET tracers have been developed and introduced into clinical practice. 68Ga-Fibroblast Activation Protein Inhibitor (FAPI) has been studied in the diagnosis of various malignant and nonmalignant diseases; it targets fibroblast activation protein (FAP) and thus reflects the distribution of cancer-associated fibroblasts (CAFs). However, its clinical significance in AAV remains to be further investigated. This study aims to use a CAF-targeted novel PET tracer to conveniently and noninvasively detect the real-time distribution of lesions in patients, providing valuable information for personalized diagnosis and treatment.

CONDITIONS

Official Title

(68)Ga-FAPI PET/CT in Patients With ANCA-associated Vasculitis

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Meet the 2022 ACR/EULAR criteria for ANCA-associated vasculitis
  • Diagnosed with interstitial lung disease based on HRCT images from within one year
  • Complete clinical information available
  • Signed informed consent form
  • Willing to follow study procedures throughout the trial
Not Eligible

You will not qualify if you...

  • Have other rheumatic diseases
  • Have other diseases that may cause interstitial lung disease or kidney problems, such as lupus, dermatomyositis, or rheumatoid arthritis
  • History of or planned hematopoietic stem cell transplantation
  • Severe health problems like serious heart, lung, bone marrow, liver, or kidney issues
  • Acute abdominal emergencies like intestinal perforation or blockage
  • Pregnant, possibly pregnant, or breastfeeding women
  • Poor treatment compliance

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ruiiin Hospital Shanghai JiaoTong University School of Medicine

Shanghai, China, 200025

Actively Recruiting

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Research Team

H

Hong-Lei Liu

CONTACT

J

Jiajia Hu

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

4

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