ISRCTN98284169已完成不适用
A double-blind, randomised, controlled multicentre trial of misoprostol treatment prior to Vacuum Aspiration for termination of early pregnancy
DP/UNFPA/WHO/World Bank - Special Programme of Research, Development and Research Training in Human Reproduction0 个研究点目标入组 4,984 人开始时间: 2007年5月3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
- 4,984
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 requesting abortion and eligible for legal termination of normal single intrauterine pregnancy of less than 12 completed weeks (84 days) of gestation
- •2. Consent to participation
- •3. Able to understand information on the study
- •4. Agree to return for the scheduled follow-up visit
排除标准
- •Women are not eligible if they have:
- •1. A medical condition or disease that requires special treatment, care of precautions in conjunction with vacuum aspiration
- •2. Allergy to misoprostol
- •3. Contraindications to misoprostol
- •4. Anaemia or any coagulation disorder
研究者
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