IRCT2015020715795N2已完成2 期
Comparison of intravenous syntocinon in the third stage of labor with rectal misoprostol abortions after the second trimester of pregnancy
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 100
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
- 年龄范围
- no limit 至 no limit（—）
- 性别
- Female
入选标准
- •Inclusion criteria were: legal permission to go to the end of pregnancy; intrauterine fetal death; gestational age 14 to 18 weeks; premature rupture approved exclusion criteria of the study: allergy or intolerance known as misoprostol; high blood pressure 160/90; severe cardiovascular disease; the patient's general condition is very bad; history of previous uterine scar (except single layer lower uterine segment caesarean section with a transverse incision); severe anemia; coagulation; anticoagulation; active liver disease; uncontrolled seizure disorders; Addison's disease; steroid use
排除标准
- 未提供
研究者
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