Actively Recruiting
Use of a New PET Scan Targeting Fibroblast Activation Protein in Adults with ANCA-Associated Vasculitis to Detect Lung and Kidney Involvement
Led by Ruijin Hospital · Updated on 2025-11-17
30
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating antineutrophil cytoplasmic antibody ANCA-associated vasculitis AAV, a condition where lung and kidney involvement often leads to worse outcomes. This study aims to evaluate a new PET imaging tracer, 68Ga-Fibroblast Activation Protein Inhibitor FAPI, which targets activated fibroblasts to detect disease activity and lesion distribution in AAV patients. Early and accurate diagnosis using this novel tracer could help personalize treatment and better assess disease severity and prognosis. The study will observe patients with AAV, including those with or without interstitial lung disease and renal dysfunction, using the 68Ga-FAPI PETCT scan. This noninvasive imaging technique allows whole-body disease localization in a single exam. The study will compare disease severity and activity as measured by the PETCT scan within four weeks after enrollment. No experimental treatments are administered since this is an observational study. Participants will undergo clinical evaluations and the PETCT imaging to assess disease activity and severity. Researchers will collect clinical information and imaging data to provide insights on lesion distribution and organ involvement. The study requires informed consent and cooperation throughout the process. Total participation time varies, with the primary outcome measured within four weeks post-enrollment. Safety and compliance will be monitored during the study period, which runs until July 2028.
CONDITIONS
Brief 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 classification criteria for ANCA-associated vasculitis
- Diagnosed with interstitial lung disease based on high-resolution CT images within one year prior to enrollment
- Have complete clinical information available
- Provide signed and dated informed consent
- Willing to comply with study procedures and cooperate throughout the study
You will not qualify if you...
- Have other rheumatic diseases
- Have other conditions causing interstitial lung disease or kidney impairment such as systemic lupus erythematosus, dermatomyositis, or rheumatoid arthritis
- History of or planned hematopoietic stem cell transplantation
- Severe comorbidities like severe cardiopulmonary insufficiency, bone marrow suppression, or liver/kidney failure
- Acute abdominal emergencies such as intestinal perforation or obstruction
- Pregnant, potentially pregnant, or breastfeeding women
- Poor treatment compliance
Research Team
H
Hong-Lei Liu
J
Jiajia Hu
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