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临床试验/CTRI/2017/10/010009
CTRI/2017/10/010009尚未招募不适用

Clinical and neuro-imaging correlates in hypertensive disorders of pregnancy

AIIMS Bhubaneswar1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2017年1月11日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
30
试验地点
1
主要终点
Co-relation of clinical, laboratory and neuro-imaging parameters in hypertensive pregnant women

研究概览

简要总结

Hypertensive disorders of pregnancy are a known cause of adverse maternal and foetal outcomes. Various findings with magnetic resonance imaging (MRI) findings in pre-eclampsia & eclampsia include symmetrical occipital lesions suggestive of posterior reversible encephalopathy syndrome (PRES) and generalized vasospasm. Higher levels of lactate dehydrogenase (LDH) have been found in women with brain edema on MRI and also, other factors like serum aminoaspartate (AST) and diastolic blood pressure have been found to be predictive of MRI changes. However, very few studies are there which have attempted co-relation of all these parameters with neuro-imaging. Against this background, this current study will attempt to co-relate clinical and laboratory findings with neuro-imaging in women with hypertensive disorders of pregnancy, especially, pre-eclapmsia and ecmlapsia and also study the maternal and foetal outcomes during the hospital stay.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • All pregnant women with a diagnosis of hypertensive disorder of pregnancy (pre-eclampsia, eclampsia, chronic hypertension, pre-eclampsia superimposed on chronic hypertension, gestational hypertension) will be recruited into the trial after obtaining consent.

排除标准

  • Pregnant women with epilepsy, malaria, cerebral infections and metabolic disorders will be excluded.

结局指标

主要结局

Co-relation of clinical, laboratory and neuro-imaging parameters in hypertensive pregnant women

时间窗: Upto 7 days postpartum

次要结局

  • Maternal and foetal outcomes(Upto 7 days postpartum)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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