跳至主要内容
临床试验/NCT03882099
NCT03882099Unknown不适用

Vitamin D Level in Patients With Pre-eclampsia, Eclampsia and Normal Full Term Pregnant

Cairo University1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2019年3月17日最近更新:
适应症

试验速览

阶段
不适用
入组人数
500
试验地点
1
主要终点
To compare vitamin D levels in the three groups

研究概览

简要总结

To compare 25(OH)D level in patients with pre-eclampsia, eclampsia and normotensive pregnant women as well as to study the prevalence of Vitamin D deficiency among the 3 groups.

详细描述

200 patients with pre-eclampsia, 100 with eclampsia and 200 normotensive pregnant controls attending Delivery/emergency department in Kasr Al Ainy hospital will be included in the study (from March 2019 till September 2019). 25(OH) D level will be measured for the three groups.

  • Preeclampsia is defined as systolic BP >140 and/or diastolic BP>90 on two occasions, 4 hours apart in pregnant females>20 weeks, plus proteinuria >/= 1+ urine dipstick protein.
  • Eclampsia defined as tonic-clonic seizures in women with pre-eclampsia.
  • Controls are normotensive pregnant females with no proteinuria and no other medical disorders.
  • The determination of 25(OH) D is based on a competitive enzyme-linked immunosorbant assay (ELISA) using the 25(OH)D3/D2 ELISA system (ORGENTIC DIAGNOSTIKA GmbH, Germany)

Inclusion criteria:

Age 20-35 years Gestational age 30-40 weeks

Exclsion criteria:

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
20 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age 20-35 years
  • Gestational age 30-40 weeks

排除标准

  • Twin pregnancy
  • Other medical conditions during pregnancy
  • Drugs that influence Vit D levels eg.antiepileptics and antituberculous treatment

结局指标

主要结局

To compare vitamin D levels in the three groups

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yahia El-Faissal

Dr

Cairo University

研究点 (1)

Loading locations...

相似试验