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Clinical Trial Summary

The purpose of this study is to explore the inflammatory biomarkers for the diagnosis of obstetric posterior reversible encephalopathy syndrome.


Clinical Trial Description

The investigators retrospectively collected data (General information, clinical data, biochemical indicators, imaging features, and pregnancy outcome) from pregnant woman diagnosed with PRES to explore the inflammatory biomarkers for the diagnosis of oPRES during 2012 to 2021.Then, the investigators grouped all the patients into PRES group (PE or E with PRES) and NOT-PRES group (PE or E without PRES) according to the diagnostic criteria of PRES. Then, the investigators analysed the inflammatory biomarkers, such as neutrophil-lymphocyte ratio (NLR), platelet-lymphocyte ratio (PLR), monocyte-lymphocyte ratio (MLR), and so on of two groups, and compared the difference of tow groups. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05433870
Study type Observational
Source Guangzhou Medical University
Contact
Status Completed
Phase
Start date July 1, 2022
Completion date July 31, 2022

See also
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Recruiting NCT04950270 - Copeptin Kinetics in Critically Ill Patients With Posterior Reversible Encephalopathy Syndrome
Not yet recruiting NCT05140850 - Long-term Consequences of Neuroimaging and Perceived Cognitive Dysfunction in oPRES
Recruiting NCT02665598 - Prognostic Observation of Posterior Reversible Encephalopathy Syndrome
Completed NCT05310513 - The Predictors of ICU Admission of oPRES