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临床试验/NCT02145767
NCT02145767已完成2 期

Progesterone for the Prevention of Miscarriage and Preterm Birth in Women With First Trimester Bleeding: PREEMPT Trial

Sir Mortimer B. Davis - Jewish General Hospital7 个研究点 分布在 1 个国家目标入组 850 人开始时间: 2014年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
850
试验地点
7
主要终点
Miscarriage

研究概览

简要总结

Miscarriages and preterm births are common and serious events affecting women, families, and healthcare systems on many levels. One of the risk factors for miscarriage and preterm birth is bleeding in the first trimester of pregnancy. Progesterone, a hormone that plays a key role during pregnancy, has been proposed as a possible medication to be used in pregnancy to prevent miscarriage and preterm birth among women who have bleeding in their first trimester of pregnancy. Unfortunately, unless sound clinical evidence is obtained through a clinical trial, whether or not progesterone can indeed prevent miscarriage and preterm birth remains uncertain and thus is not a recommended treatment in women with early pregnancy bleeding. The purpose of our study is to evaluate the effect of progesterone for the prevention of miscarriage and preterm birth among women with early pregnancy bleeding. We will carry out a clinical trial in which 850 women will be randomized to receive either progesterone supplementation (425 women) or a similarly appearing placebo (425 women) and the outcome of their pregnancy will be compared.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Live intrauterine singleton pregnancy of <14 weeks by crown-rump length on ultrasound with documented fetal cardiac activity
  • Presence of a perigestational (subchorionic) hemorrhage on ultrasound

排除标准

  • Contraindication to Progesterone
  • Any indication for progesterone

研究组 & 干预措施

Progesterone

Experimental

Progesterone 200mg suppository administered vaginally at bedtime until 34 completed weeks of pregnancy.

干预措施: Progesterone (Drug)

Placebo

Placebo Comparator

Similar appearing suppository containing vehicle alone administered vaginally at bedtime until 34 completed weeks of pregnancy.

干预措施: Placebo (Drug)

结局指标

主要结局

Miscarriage

时间窗: From 6-8 weeks of pregnancy until miscarriage

Occurrence of a miscarriage (\<20 weeks)

Preterm birth

时间窗: From 6-8 weeks of pregnancy until delivery

Occurrence of preterm birth (\<37 weeks)

次要结局

  • Maternal outcomes(From 6-8 weeks of pregnancy until 6 weeks post delivery)
  • Neonatal outcomes(2 days to 6 weeks post delivery)
  • Healthcare outcomes(From 6-8 weeks of pregnancy until 6 weeks post delivery)

研究者

发起方
Sir Mortimer B. Davis - Jewish General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Haim Abenhaim

Obstetrician & Gynecologist, Maternal Fetal Medicine Specialist, Director of Perinatal Research

Sir Mortimer B. Davis - Jewish General Hospital

研究点 (7)

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