IRCT201210093706N15已完成未知
The effect of supplementation on the combined pill continuation rate and Harassment rate of its side effects: a randomized controlled trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 330
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
- 15 years 至 49 years（—）
- 性别
- Female
入选标准
- •married no pregnant women aged 18-40 years; intention to start using Low dose (LD) combined pills as a contraceptive method; being literate; not taking combined hormonal methods at least in the past three months.
- •Exclusion criteria: plan to get pregnant in 6 months; not having medical eligibility criteria for contraceptive use.
排除标准
- 未提供
研究者
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