IRCT20201218049749N1已完成3 期
A comparison of vaginal misoprostol and vaginal evening primrose oil in first trimester termination
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 72
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
- •Pregnant women go to Beheshti Hospital for up to 14 weeks to terminate their pregnancy
排除标准
- •Uncontrolled seizures
- •Uncontrolled blood pressure
- •Chronic lung disease
- •Mitral valve stenosis
- •History of known allergy to prostaglandin E1
- •Inflammatory bowel disease
- •Sensitivity to evening primrose
- •Coagulation disease
- •Schizophrenia and phenothiazine use
- •Cone biopsy of the cervix
- •Smoking and supplements
研究者
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