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Clinical Trial Summary

The main objective is to analyze the abnormality of physical condition, mental health and blood examination of the patients with benign paroxysmal positional vertigo (BPPV). Besides, the investigators aim to establish a database of BPPV based on multimodal magnetic resonance imaging data in the brain to identify high-risk patients with residual dizziness (RD) and systematically establish the comprehensive assessment system for the precise diagnosis, treatment and recovery of RD, optimize the tactics of BPPV management in China.


Clinical Trial Description

This is an observational, longitudinal, and single-center study. Confirmed BPPV cases will complete the following programs before and after 1 and 6 months of treatment for exploring biological mechanism and predictive biomarkers of BPPV: 1) fill in the behavioral psychological scales, 2) submit blood samples at a local laboratory, 3) receive 3 times brain MRI scan. The healthy controls will complete the same programs as BPPV-group mentioned above only at the time of inclusion. The investigators will establish the brain MRI database containing neuropsychological scales and blood parameters of BPPV in China. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06228196
Study type Observational
Source First Affiliated Hospital Xi'an Jiaotong University
Contact Yuan Wang, M.D.
Phone 0086-13324598144
Email wangyuan8003@126.com
Status Recruiting
Phase
Start date January 8, 2024
Completion date September 30, 2026

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