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临床试验/NCT01200186
NCT01200186已完成不适用

Non-interventional Study on Oral Contraception Not Containing Ethinylestradiol (EE) to Assess Continuation Rates and Satisfaction

Bayer0 个研究点目标入组 3,258 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Bayer
入组人数
3,258
主要终点
The primary outcome measure will be time-to-event for discontinuation due to bleeding irregularities.

研究概览

简要总结

Prospective, non-interventional, multi-center study. Each subject will be followed for up to twelve months during the treatment with oral hormonal contraceptives(Qlaira ® or a Progestin Only Pill). For each subject demographic data and medical history will be documented at Visit 1: (Baseline). Bleeding profile, subjective assessment of study treatment (satisfaction and wellbeing) and adverse events including unintended pregnancies will be documented at Visit 2 (Month 3-5) and Visit 3 (Month 6-12). Data audit/monitoring will be done.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women between 18-50 years
  • Women who used ethinylestradiol containing oral contraceptives for at least the three preceding months before the study
  • Women who decided to start Qlaira® or a Progestin Only Pill. The prescription of the hormonal contraceptive is made at the discretion of the attending physician and has to be documented

排除标准

  • Contraindications and warnings of the respective Summary of Product Characteristics (Qlaira® or Progestin Only Pill)
  • Women who are breast-feeding

研究组 & 干预措施

Group 1

干预措施: EV/DNG (Qlaira, BAY86-5027) (Drug)

Group 2

干预措施: Progestin Only Pills (Drug)

结局指标

主要结局

The primary outcome measure will be time-to-event for discontinuation due to bleeding irregularities.

时间窗: up to 12 Months

次要结局

  • Number of heavy and/or prolonged bleeding(Month 6-12)
  • Number of intracyclic bleeding(Month 6-12)
  • Global assessment of well-being and satisfaction(Month 6-12)
  • Adverse events (AEs) at any time point, whether or not related to the therapy or reference therapy(up to 12 Months)
  • Time to event for discontinuation due to reasons other than bleeding irregularities(Month 6-12)
  • Number of unintended pregnancies(Month 6-12)
  • Discontinuation rate for the following reasons: Occasional absent or persistent absent withdrawal bleeding , intracyclic bleeding, heavy and/or prolonged bleeding, other medical reasons, non-medical reasons(Month 6-12)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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