Actively Recruiting
(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
Eligibility Criteria
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
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
Trial Site Locations
Total: 1 location
1
Ruiiin Hospital Shanghai JiaoTong University School of Medicine
Shanghai, China, 200025
Actively Recruiting
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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