ISRCTN85124072已完成未知
A randomised controlled trial of oral versus vaginal misoprostol for medical management of early foetal demise
South Tees Hospitals NHS Trust (UK)0 个研究点目标入组 240 人开始时间: 2009年4月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 240
研究概览
简要总结
2009 results in: https://obgyn.onlinelibrary.wiley.com/doi/abs/10.1016/S0020-7292%2809%2961912-3 (added 24/10/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •Women with an ultrasound diagnosis of (singleton) early foetal demise, with no medical contraindications or known allergy to misoprostol or mifepristone.
排除标准
- •1. Heavy smokers (of >20 cigarettes day)
- •2. Aged >35 years
- •3. Severe asthma
- •4. Cardiovascular disease, hypertension (blood pressure [BP] >160/100 mmHg)
- •5. Chronic adrenal, renal or hepatic failure
- •6. Porphyria or haemorrhagic disorders
- •7. Long term corticosteroid
- •8. Anticoagulant or non-steroidal anti-inflammatory drug (NSAID) therapy
- •9. Known allergy to mifepristone or misoprostol
研究者
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