PACTR201801002743482尚未招募未知
Comparative long-term effects of depot medroxyprogesterone acetate, a levonorgestrel implant and a copper intrauterine device on depression and sexual dysfunction: An ancillary study of the ECHO* randomised trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 291
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
- •¿16 to 35 years of age
- •¿HIV sero-negative at baseline
- •¿Seeking effective contraception
- •¿Able and willing to provide written informed consent
- •¿Agrees to be randomised to either the copper IUD, DMPA, or LNG implant
- •¿Agrees to use assigned method for 18 months
- •¿Agrees to follow all study requirements
- •¿Intends to stay in the study area for the next 18 months and willing and able to provide adequate locator information
- •¿If has had a recent third trimester birth, is at least 6 weeks¿ postpartum
- •¿Is sexually active (has had vaginal sex within the last 3 months) or has been pregnant within the last 3 months
- •¿Agrees not to participate in studies of drugs or vaccines or any other clinical research study while participating in this study
排除标准
- •Women are not eligible to participate if they have medical contraindications to the IUD, DMPA, or LNG implant (WHO Medical Eligibility Criteria category 3 or 4),
研究者
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