ACTRN12609000391279
招募中
4 期
Comparative 12 month study of menstrually-signalled use of an ethinyl oestradiol and levonorgestrel low-dose pill and a low-dose contraceptive vaginal ring containing ethinyl oestradiol and etonogestrel to assess the number of bleeding spotting days
概览
- 阶段
- 4 期
- 干预措施
- 未指定
- 疾病 / 适应症
- Contraception
- 发起方
- Family Planning NSW
- 入组人数
- 140
- 状态
- 招募中
- 最后更新
- 6年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Can be new users, restarters or switchers
- •No contraindications to combined hormonal contraceptive use
- •Willing to give informed consent to randomisation
- •Willing to be contacted monthly by research assistant and to maintain a menstrual chart
- •Willing to have a blood samples taken at inclusion and completion of study for biochemical and haematological testing.
- •Willing to keep account of sanitary protection used and cost over duration of study.
排除标准
- •Currently pregnant or trying to get pregnant.
- •Sterilisation.
- •Contraindications to combined hormonal contraceptive use
- •Smokers aged \= 35 years and over are excluded
- •Depot medroxyprogestogen acetateuse within last six months
- •Undiagnosed intermenstrual bleeding
- •Problems with cycle control whilst taking combined oral contraceptives leading to discontinuation
- •Unwilling to stop taking non\-steroidal anti\-inflammatory drugs
- •Taking any concomitant medications which cause enzyme induction and could effect steroidal blood levels
结局指标
主要结局
未指定
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