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Clinical Trials in China / NCT06228196
Recruiting Observational

Cohort Study of Clinical and Neuroimaging Characteristics for BPPV Patients in China

NCT06228196 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital Xi'an Jiaotong University
Phase
Observational
Started
2024-01-08
Last updated
2024-02-26

Condition(s) studied

BPPVVertigoVertigo, Peripheral

Investigational drug(s) / intervention(s)

Simultaneous cortico-spinal magnetic resonance imaging, Serum

Simultaneous cortico-spinal magnetic resonance imaging, Serum: Simultaneous cortico-spinal magnetic resonance imaging data were collected in a strong magnetic field and collected the serum of participants.

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Confirmed diagnosis of BPPV/Healthy subjects who have not had BPPV Exclusion Criteria: * History of organic diseases in central nervous system and mental disorder, such as tumors, infections, depressive disorder, schizophrenia, etc. Claustrophobic

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The First Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi Recruiting

More First Affiliated Hospital Xi'an Jiaotong University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06228196 on ClinicalTrials.gov ↗ ← All trials in China