PACTR201210000420221已完成未知
A randomised control trial studying the effects of the copper intrauterine device and injectable progestogen contraceptive on depression and sexual functioning of women in the Eastern Cape
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 200
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
- 18 Year(s) 至 35 Year(s)（—）
- 性别
- Female
入选标准
- •Women of child bearing age between 18 to 35 years
- •Women with no evidence of active pelvic infection
- •Women who have no contraindications to injectable Progestogen or IUD
- •Women who are prepared to use either method of contraception
- •Women delivered less than 48 ago.
- •Women who are willing and able to give consent.
排除标准
- •Recent noticed vaginal bleeding that is unusual.
- •Any contraindication for deport injection and IUD as stated on the WHO contraceptive eligibility criteria will.
- •Women at baseline screening with depression score of 29 - 63(severe depression)
- •Women with no access to telephone
研究者
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