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临床试验/CTRI/2024/07/070822
CTRI/2024/07/070822招募中Unknown

A Clinical Performance Evaluation Case-Control Study for Point-of-Care Preeclampsia Screening Kit in Pregnant Women - NI

Intignus Biotech Pvt. Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方

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

入选标准

  • Pregnant women aged 18 years and above with confirmed diagnosis of preeclampsia based on ACOG guidelines
  • Age and time-matched normotensive pregnant women aged 18 years and above

排除标准

  • Patients meeting any of the following exclusion criteria will not be eligible for participation in this study:
  • 1. Unconscious or severely ill status
  • 2. Having major fetal abnormality identified at the time of enrollment
  • 3. Known bleeding disorder such as von Willebrand’s disease, peptic ulceration
  • 4. Participation in another drug trial within 28 days before screening
  • 5. Unable to provide written informed consent

研究者

发起方
Intignus Biotech Pvt. Ltd

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