跳至主要内容
临床试验/NCT01198444
NCT01198444已完成不适用

Prospective, Open-label Observational Survey Evaluating Patients Compliance to Administration Regimen During Low Dose Combined Oral Contraceptive Use in Everyday Praxis Data on Oral Contraceptives Compliance - DOC Study

Bayer0 个研究点目标入组 11,884 人开始时间: 2007年12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
11,884
主要终点
The percentage of users showing noncompliant behaviors

研究概览

简要总结

Adherence to the dosing scheme is the principal element of Combined Oral Contraceptives efficiency. On the other hand noncompliance seemed to be an inseparable element of any oral treatment. The aim of the study is to evaluate in everyday practice the relation between dosage errors and indicated factors, potentially influencing the compliance with the dosing scheme.

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

  • Patients at the age of over 18 requiring contraception. The decisions would be made at the discretion of the attending physician.

排除标准

  • According to official Summary of Product Characteristics (SmPC) contraindications.

研究组 & 干预措施

Group 1

干预措施: EE/DRSP (Yasmin Product Family) (Drug)

结局指标

主要结局

The percentage of users showing noncompliant behaviors

时间窗: 3 consecutive cycles

次要结局

  • The characteristics of noncompliant behavior(3 consecutive cycles)
  • The relation between noncompliant behavior and selected factors(3 consecutive cycles)

研究者

发起方
Bayer
申办方类型
Industry

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