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临床试验/NCT07464379
NCT07464379招募中不适用

Collect Blood Pressure, Blood, Amniotic Fluid, Placenta and Other Samples From Normal Pregnant Women, Patients With Pregnancy-induced Hypertension and Those Who Have Experienced Miscarriage, and Conduct Tests on Them.

Second Affiliated Hospital of Wenzhou Medical University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2020年1月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
100
试验地点
1
主要终点
PIH

研究概览

简要总结

Collect blood pressure, blood, amniotic fluid, placenta and other samples from normal pregnant women, patients with pregnancy-induced hypertension and those who have experienced miscarriage, and conduct tests on them.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • - Healthy pregnant women, patients with miscarriage, etc.

排除标准

  • Heart disease, infections, etc. in pregnant women Uncooperative patients

研究组 & 干预措施

control group

Healthy pregnant women

干预措施: no Intervention (Other)

PIH group

Pregnancy-induced hypertension patients

干预措施: no Intervention (Other)

结局指标

主要结局

PIH

时间窗: Early pregnancy:Weeks 1 to 12 (the first to third months of pregnancy) ;mid-pregnancy:Weeks 13 to 27 (the 4th to 6th month of pregnancy) ;post-delivery period:Weeks 28 to 40 (the 7th to 9th months of pregnancy);the day of delivery。

the content of GPR18 type macrophages

次要结局

  • PIH(delivery)

研究者

发起方
Second Affiliated Hospital of Wenzhou Medical University
申办方类型
Other
责任方
Sponsor

研究点 (1)

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