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Characterisation of lipoproteins from patients with preeclampsia compared to healthy, pregnant and healthy, non-pregnant women

niversitätklinikum Freiburg Institut für Klinische Chemie und Laboratoriumsmedizin0 个研究点目标入组 155 人开始时间: 2013年11月5日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
155

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
Female

入选标准

  • Group 1 (case): Pregnant women with preeclampsia according to the criteria of the German Society of Gynaecology and Obstetrics: hyptertension in pregancy (RR>140/90mmHg) and proteinuria (>300 mg/24h) occuring after the 20th week of pregnancy. Preeclampsia can also be diagnosed without proteinuria if fetal growth restriction, liver involvement, renal insufficiency, neurological dysfunctions or hematological disorders are observed after the 20th week of pregnancy. Informed consent. Age >18 years. Group 2 (control): for every individual from group 1 a healthy, pregnant women in matching gestational age (+/- 1 week). Informed consent. Age > 18 years. Group 3 (control): Healthy, non pregnant women. Informed consent. Age > 18 years and < 45 years.

排除标准

  • Group 1 (case): lack of informed consent. Group 2 and 3 (controls): lack of informed consent. By anamnesis detection of: arterial hypertension, treatment with antihypertensive agents and other cardiac drugs, diabetes mellitus, renal insufficiency, lipid disorders, liver diseases.

研究者

发起方
niversitätklinikum Freiburg Institut für Klinische Chemie und Laboratoriumsmedizin

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