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临床试验/NCT00883662
NCT00883662已完成不适用

Mirena Observational Program

Bayer0 个研究点目标入组 2,725 人开始时间: 2009年5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
2,725
主要终点
Patient distribution per indication

研究概览

简要总结

Mirena is used for long-term in Kazakhstan, and in our observational program we would like to study patients distribution per indications of Mirena, and also patient compliance within a year after Mirena insertion. For patients with all approved indications for Mirena use: contraception, treatment of menorrhagia and protection from endometrial hyperplasia during estrogen replacement therapy

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

入选标准

  • Patients older than 18 years with previously taken decision of their gynecologist to insert Mirena according to registered indications

排除标准

  • All patients with contraindications to Mirena insertion, according to approved prescribing information.

研究组 & 干预措施

Group 1

干预措施: Levonorgestrel (Mirena, BAY86-5028) (Drug)

结局指标

主要结局

Patient distribution per indication

时间窗: 12 months

次要结局

  • Patient compliance(12 months)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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