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临床试验/TCTR20220527007
TCTR20220527007已完成不适用

Effects of Vaginal Progesterone on Prevention of Preterm Delivery in Pregnant Women with Prior Spontaneous Preterm Birth

/A0 个研究点目标入组 82 人开始时间: 2022年5月27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
82

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
N/A (No limit) 至 N/A (No limit)(—)
性别
Female

入选标准

  • 1.Singleton pregnancy
  • 2.History of Prior Spontaneous Preterm Birth
  • 3.First visit at antenatal care unit of Rayong hospital before 16 weeks gestational age
  • 4. Use vaginal progesterone

排除标准

  • 1.Start vaginal progesterone after gestational age 18 week
  • 2. Loss follow up or denied use vaginal progesterone continueusly
  • 3. The Fetus had severe anormally or genetic syndrome that need temination of prenancy
  • 4. Problem of cervix uteri or Uterus such as congenital malformaion, Status post LEEP, Emdometriosis of uterus
  • 5.Obstretric complications that need temination of prenancy such as Severe preeclampsia, Fetal distress
  • 6.Medical complications that need temination of prenancy such as heart failure, servere pulmonary disease
  • 7.Contraindication for use Progesterone

研究者

发起方
/A

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