ACTRN12614000889651撤回未知
Comparison of desogestrel and levonorgestrel releasing intrauterine device in terms of menstrual pattern, side effects and patient satisfaction in postpartum contraception
Mine Kiseli0 个研究点目标入组 112 人开始时间: 2014年8月21日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 撤回
- 发起方
- 入组人数
- 112
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 45 Years（—）
- 性别
- Female
入选标准
- •Patients who were prescribed oral desogestrel or who were applied levonorgestrel releasing intrauterine device for postpartum contraception
- •Six weeks passed after vaginal birth and 8 weeks passed after cesarean section
- •Patients giving consent for the participation to the study
排除标准
- •History of acute artery or vein thrombosis
- •6 months passed after the delivery
- •Women with acute or chronic liver disease, diabetes, hypertension or renal disease
- •Women having postpartum depressive symptoms
- •Patients who won't give consent for the participation
研究者
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