EUCTR2014-001243-20-FI进行中(未招募)不适用
Syntethic vs. natural estrogen in combined oral contraception- effect on insulinsensitivity, inflammation, coagulation and endometrium. A comparison with a progestin-only preparation. - SYLVI
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
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
- •woman aged 18-35, normal weight BMI 19-24.9 kg/m2, good general health: no diagnosed disease or regular medications, regular mentrual cycle (21-35 days), prior to entering the study min. 2 months wihout hormonal contraception, no contraindications for the use of hormonal oral combined contraception
- •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 60
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •abnormal results in 2h oral glucose tolerance test, abnormal findings in gyneacological exam (inc. sonography), blood pressure >140/90 mmHg, regular (daily) smoking, alcohol or drug abuse
研究者
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