The purpose of this study is to determine the features of clinical imaging, disease severity and pregnancy outcomes in posterior reversible encephalopathy syndrome with preeclampsia or eclampsia.
Age range
16 Years – 50 Years
Sex
FEMALE
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
features of clinical imaging
Timeframe: Cranial Imaging was examined immediately at the onset of symptoms, such as s headaches, visual changes, seizures, consciousness impairment, mental disorders, and focal neurological deficits.
blood pressure(BP)
Timeframe: The BP of patients was obtained immediately at the onset of symptoms.
biochemical parameters
Timeframe: Biochemical indicators were collected within 1 week of the hospital stay.
pregnancy outcomes
Timeframe: The pregnancy outcomes will record immediately when the patients deliver.
pregnancy outcomes
Timeframe: From day of admission until the day of discharge or date of death from any cause,whichever came first,assessed up to 1 year.