DRKS00025993尚未招募不适用
Observational study to evaluate acceptability and bleeding profile with Drospirenone 4 mg, in a regimen of use 24/4 in contraception (Slinda®, Exeltis HealthCare) after six months of use. - EXELINDA
Exeltis Healthcare0 个研究点目标入组 300 人开始时间: 2021年8月6日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 300
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 50 Years（—）
- 性别
- Female
入选标准
- •1.Women over 18 years up to 50 years.
- •2. They use Slinda ® for the approved indication (contraception) and have started treatment at least 6 months before the visit.
- •3. They shall give informed consent in order to participate in the study.
排除标准
- 未提供
研究者
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