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临床试验/NCT03292939
NCT03292939已完成2 期

The Effect of Vaginal Progestrone on Fetal and Maternal Doppler Indices

Kasr El Aini Hospital2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2017年1月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
80
试验地点
2
主要终点
change of ultrasound doppler indices.

研究概览

简要总结

The aim of our study is to assess the effect of vaginal progestrone on fetal and maternal doppler indices

详细描述

A complete Doppler flow assessment of the maternal and fetal circulation was conducted by an independent investigator blinded to the treatment, before and 48 hours after the first administration of 400mg of vaginal progesterone, Voluson E8 (GE Healthcare, Zipf, Austria) ultrasound machine,equipped with a 3.5- MHz curvilinear abdominal transducer with color imaging capabilities, was used in all cases.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

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

  • Gestational age: 18-33 weeks
  • Willing and able to give informed consent
  • History of preterm labor (<34 weeks)
  • At risk for preterm labor ( increased amniotic fluid volume)
  • Short cervical length (<25mm) as incidental finding
  • Presenting with actual cervical changes ( dilatation and\or effacement) in current pregnancy

排除标准

  • Contraindication to progesterone use
  • Diabetic patients, have glucose intolerance
  • Multiple pregnancies

研究组 & 干预措施

vaginal progestrone group

Other

cohort of patients who received 400mg vaginal progestrone .

干预措施: A complete Doppler flow assessment of the maternal and fetal circulation (Diagnostic Test)

结局指标

主要结局

change of ultrasound doppler indices.

时间窗: before and 48 hours after progestrone admistration

A complete Doppler flow assessment of the maternaland fetal circulation was conducted by an independent investigator blinded to the treatment, before and 48 hours after the first administration of progesterone, Voluson E8 (GE Healthcare, Zipf, Austria) ultrasoundmachine,equippedwitha3.5-MHzcurvilinearabdominaltransducer with color imaging capabilities, was used in all cases.

次要结局

未报告次要终点

研究者

发起方
Kasr El Aini Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

sarah mohamed hassan

lecturer of obstetrics and gynecology Cairo university

Kasr El Aini Hospital

研究点 (2)

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Progestrone and Doppler Indices | 临床试验