EUCTR2019-002138-35-NL进行中(未招募)1 期
Heavy menstrual bleeding in premenopausal women treated with direct oral anticoagulants - the MEDEA study - MEDEA
Amsterdam University Medical Centers - location AMC0 个研究点目标入组 120 人开始时间: 2019年11月12日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •- premenopausal women
- •- age =18 years
- •- anticoagulant treatment with a factor Xa inhibitor
- •- indication for anticoagulant treatment >3months after inclusion
- •- heavy menstrual bleeding and a PBAC-score >150
- •- use of adequate contraceptive methods during study participation (this is advised to any woman on factor Xa inhibitors during fertile ages, regardless of study participation)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 120
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- PBAC-score =150
- •- postmenopausal women; women >12 consecutive months of spontaneous amenorrhea
- •- concomitant use of hormonal therapy as a new intervention for HMB
- •- pregnancy or currently planning for pregnancy
- •- active malignancy or treatment with chemotherapy/radiotherapy
- •- cervical preneoplastic lesions
- •- contra indication for the registered products dabigatran or tranexamic acid
- •- any condition that, as judged by investigator, would place the subject at an increased risk of harm if she participated in the study
研究者
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