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临床试验/CTRI/2024/07/069840
CTRI/2024/07/069840尚未招募不适用

An observational study of coagulation profile in severe pre-ecampsia and eclampsia patients.

Spurthi Prabhakar self1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年7月13日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
74
试验地点
1
主要终点
platelet count decreases

研究概览

简要总结

The  study is being conducted so as to observe the blood parameters like platelet count, PT ,APTT , serum fibrinogen, D-Dimer in severe pre- eclampsia and eclampsia patients . With pthe help of these parameters we will detect thrombocytopenia and coagulation failure early  and manage its complications before it worsens.

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

  • hypertensive females.

排除标准

  • pregnant female with known history of pre hypertensive disorder on anticoagulant therapy established DIC intrauterine fetal demise.
  • history of bleeding disorder abruptio placentae.

结局指标

主要结局

platelet count decreases

时间窗: The values will be observed in period of gestation between 20 weeks to 40 weeks , in the above gestational period whenever patients arrives with symptoms of severe pre eclampsia and eclampsia

PT and APTT is prolonged

时间窗: The values will be observed in period of gestation between 20 weeks to 40 weeks , in the above gestational period whenever patients arrives with symptoms of severe pre eclampsia and eclampsia

次要结局

未报告次要终点

研究者

发起方
Spurthi Prabhakar self
申办方类型
Other [Deemed university]
责任方
Principal Investigator
主要研究者

Spurthi Prabhakar

Jawaharlal Nehru medical college , Belgavi

研究点 (1)

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