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Clinical Trial Summary

The purpose of this study is to explore the long-term consequences of neuroimaging and perceived cognitive dysfunction in obstetrics posterior reversible encephalopathy syndrome.


Clinical Trial Description

This is a prospective study. The investigators divided the PE or E patients into two groups, namely PRES group and non-PRES group, according to diagnostic criteria . The general information(demographic data,blood pressure.etc.)and blood sample will be collected. Additionally,all patients receive neuroimaging examination(DTI,ASL,3D-TMI.etc.)and neuro-cognitive test(MMSE,MOCA,CFQ, etc.) to assess the cerebral white matter lesions and cognitive changes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05140850
Study type Observational [Patient Registry]
Source Guangzhou Medical University
Contact Dunjin Chen
Phone 18928916722
Email gzdrchen@gzhmu.edu.cn
Status Not yet recruiting
Phase
Start date January 2022
Completion date October 2023

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