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Clinical Trial Summary

1. Include qualified 50 ANCA-associated vasculitis(AAV) patients; and the first 27 patients will be divided into 3 groups with different diffused tension image (DTI) parameters and to choose the best strategy; 2. On baseline, 6 months after treatment and 24 months after treatment, the AAV patients will accomplish the Birming-ham vasculitis activity score(BVAS) besides DTI; 3. The new serum biomarkers of AAV associated peripheral neuropathy will be measured by ELISA; (4) Another cohort with 50 patients with AAV associated peripheral neuropathy who were evaluated by traditional methods (electromyogram) and compared to the patients cohort that evaluated using DTI by cost-benefit analysis


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04923074
Study type Observational
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact wenjia sun
Phone 86 15869029727
Email sunwinjoy@zju.edu.cn
Status Recruiting
Phase
Start date July 2021
Completion date July 2023

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