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临床试验/EUCTR2014-001243-20-FI
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

Helsinki University Central Hospital0 个研究点开始时间: 2014年5月20日最近更新:
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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