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临床试验/NCT00190177
NCT00190177已完成不适用

ECLAXIR:Search for an Association Between CX3CR1 V249I Polymorphism, Preeclampsia and Endothelial Injury

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 370 人开始时间: 2003年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
370
试验地点
1

研究概览

简要总结

The study hypothesis is the involvement of the couple CX3CR1/CX3CL1 in occurrence of endothelial injury in preeclampsia. According to this hypothesis, Carriers of the I249 allele who express less CX3CR1 shoud be protected against this risk. The main objective of the study is the search of an association between CX3CR1 V249I polymorphism and preeclampsia. The secondary aims are the search of an association with the most severe forms of preeclampsia and endothelial injury.

详细描述

It is a case-control multicenter study 185 caucasian pregnant women with preeclampsia and 185 paired controls without preeclampsia will be included.

The frequency of the V249I polymorphism in african black population will be determined by studying 200 subjects (100 cases and 100 controls).

The V249I polymorphism will be identified by PCR followed by enzyme digestion. Endothelial injury will be identified using three assays : von Willebrand factor, soluble VCAM-1 and thrombomodulin plasma levels.

CX3CR1 involvement in preeclampsia would have potential diagnostic and therapeutic consequences.

研究设计

研究类型
Observational
时间视角
Retrospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • cases: pregnant woman, evolutive pregnancy, preeclampsia, caucasian, consenting to the study

排除标准

  • multiple pregnancy, proteinuria > 300 mg/24h before 21th gestation week.

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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