跳至主要内容
临床试验/NL-OMON56768
NL-OMON56768尚未招募不适用

Circulating cell free DNA: the fingerprint of the Placenta - FIERCE

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
50

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

年龄范围
18 至 64(—)

入选标准

  • - Pregnant women >= 18 years and <= 45 years who are willing to participate.
  • - Sufficient understanding of Dutch in speaking and reading.
  • - Willingness to give written informed consent.
  • - Singleton pregnancy.
  • - Blood drawing (venapunction) planned for clinical purposes.
  • Two patient groups are eligible:
  • - Healthy pregnant women with an uncomplicated pregnancy (10 controls).
  • - Healthy pregnant women with a premature delivery (between 24 and <37 weeks)
  • clinically with suspicion of inflammation (20 cases).
  • Placentas from the pathology archive that can be used for research for a
  • baseline quality check:
  • - 10 placentas from an uncomplicated pregnancy (controls)
  • - 10 placentas with a premature delivery (between 24 and <37 weeks) clinically
  • with suspicion of inflammation (cases)

排除标准

  • Multiple pregnancy.
  • - Gastro-intestinal diseases, heart diseases, liver, pancreas and kidney
  • - Pre-existent diabetes mellitus.
  • - Unable or unwilling to give informed consent.
  • - Fetus with a known congenital/chromosomal abnormality.

研究者

相似试验