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临床试验/NCT06623955
NCT06623955已完成不适用

A Comparative Study of Maternal Serum Stathmin-1 Levels in Pregnancies With Preeclampsia, Severe Preeclampsia, and Healthy Controls

Başakşehir Çam & Sakura City Hospital1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2023年1月1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
84
试验地点
1
主要终点
Maternal Serum Stathmin-1

研究概览

简要总结

This study investigates maternal serum Stathmin-1 (STMN-1) levels in pregnancies complicated by preeclampsia and severe preeclampsia, compared to healthy pregnancies. The aim is to explore potential differences in STMN-1 levels among these groups to better understand its role in preeclampsia pathophysiology. Maternal serum STMN-1 levels will be measured between 32-34 weeks of gestation, and patients will be monitored until delivery to assess whether they develop preeclampsia or severe preeclampsia.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Clinical diagnosis of Preeclampsia: Defined by New-onset hypertension (Systolic Blood Pressure ≥140 mmHg and/or Diastolic Blood Pressure ≥90 mmHg) after 20 weeks of gestation, with or without proteinuria.
  • Clinical diagnosis of Severe Preeclampsia: Defined by criteria such as severe hypertension (systolic BP ≥160 mmHg or diastolic BP ≥110 mmHg), organ dysfunction (renal insufficiency, liver involvement, neurological complications), thrombocytopenia, pulmonary edema, or fetal growth restriction.
  • Control Group: Healthy pregnancies without preeclampsia

排除标准

  • Multiple Pregnancies
  • Pregestational Diabetes
  • Chronic Hypertension
  • Systemic Diseases (Chronic kidney disease, autoimmune diseases)
  • Fetal Anomalies
  • Premature Rupture of Membranes

结局指标

主要结局

Maternal Serum Stathmin-1

时间窗: Up to 8 weeks (Patients will be followed from inclusion in the study until the end of their pregnancy.)

To compare Stathmin-1 Levels between the pre-eclampsia and the control group.

次要结局

未报告次要终点

研究者

发起方
Başakşehir Çam & Sakura City Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Gökhan Bolluk

MD

Başakşehir Çam & Sakura City Hospital

研究点 (1)

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