NCT02159261已完成不适用
A Prospective Multicenter Non-interventional Study on Patients and Physicians Satisfaction of Yaz Plus
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
- 1,500
- 主要终点
- Satisfaction measured with a Likert response scale (from 1 - poor to 5 - excellent)
研究概览
简要总结
Local prospective multicenter non-comparative non-interventional observational study. It's planed to assess satisfaction of patients and physicians with results of Yaz Plus treatment for 13 cycles in real practice.
详细描述
Non-interventional, Yaz Plus, Contraception, Assess satisfaction, Russian Federation.
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 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Female patients ≥ 18 years old
- •Requiring contraception
- •Prescribed with Yaz Plus for the first time
排除标准
- •Contraindications for the use of Yaz Plus in accordance with the local product information
研究组 & 干预措施
Cohort 1
Female patients ≥ 18 years old requiring contraception.
干预措施: BAY98-7071_EE20/DRSP/L-5-MTHF (Drug)
结局指标
主要结局
Satisfaction measured with a Likert response scale (from 1 - poor to 5 - excellent)
时间窗: Up to 12 months
次要结局
- Changes in EVAPIL scale for assessment of tolerability of oral contraceptives.(Baseline to 12 months)
- Number of participants with adverse events as a measure of safety and tolerability(Up to 12 months)
研究者
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