ISRCTN97277056已完成不适用
Optimising the dose of Misoprostol for the prevention of postpartum haemorrhage: a randomised trial
niversity of Liverpool (UK)0 个研究点目标入组 60 人开始时间: 2010年5月13日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Women who have had spontaneous vaginal delivery
- •2. Women with gestational age >34 weeks
- •3. Women who give an informed written consent
- •4. Aged = 18 years
排除标准
- •1. Women with history of Postpartum Haemorrhage (PPH)
- •2. Women with history of Antepartum Haemorrhage (APH)
- •3. Women with previous caesarean section
- •4. Women with 5 or more previous deliveries at over 28 weeks
- •5. Women who have Premature Rupture of Membranes (PROM)
- •6. Women with anaemia (Hb <10g/dl)
- •7. Women who have given birth to a baby of birth weight > 4.0 Kgs
- •8. Women who have induced or augmented labour with any uterotonic drugs
- •9. Women with multiple pregnancies
- •10. Women with polyhydraminos
- •11. Women with pre eclampsia
- •12. Women with infection
- •13. Women who do not give a written consent
研究者
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