Evaluation of Anti-neutrophil Cytoplasm Antibodies Test
Launched by SOHAG UNIVERSITY · Jan 19, 2021
Trial Information
Current as of July 21, 2025
Unknown status
Keywords
ClinConnect Summary
To evaluate the performance of the recommended strategy for the detection of ANCA based on screening with antigen specific immunoassays on a number of AAV patients and relevant disease controls (i. e., patients for whom ANCA would be requested in the context of small-vessel vasculitis such as patients with infections, drug-induced diseases, connective tissue disease, etc.).
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • .All patients included must be older than 18 years and able to give informed consent.
- • Classification criteria and nomenclature for AAV are from the American College of Rheumatology
- • Serum sampling should be done before initiation of immunosuppressive treatment or no later than 2 weeks after onset of low-medium dose of immunosuppressive treatment (but this should be documented)
- Exclusion Criteria:
- • .Patients younger than 18 years old
About Sohag University
Sohag University is a distinguished academic institution located in Sohag, Egypt, committed to advancing healthcare through rigorous clinical research. As a clinical trial sponsor, the university leverages its robust infrastructure and multidisciplinary expertise to facilitate innovative studies aimed at improving patient outcomes and contributing to the global body of medical knowledge. With a focus on ethical standards and scientific integrity, Sohag University collaborates with healthcare professionals and researchers to conduct trials that address critical health issues, ensuring the advancement of evidence-based practices in the healthcare community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Miki, Kagawa, Japan
Patients applied
Trial Officials
Mai Mansour
Principal Investigator
Sohag University
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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