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临床试验/EUCTR2013-000925-30-SE
EUCTR2013-000925-30-SE进行中(未招募)1 期

How common are mood and sexual side-effects from combined oral contraceptives?

ppsala University0 个研究点目标入组 300 人开始时间: 2013年3月20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
300

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

入选标准

  • Age 18 -35 years
  • Healthy according to self-report
  • Informed consent
  • Accept to use barrier contraception during the study or has cupper IUD or has been sterilized
  • 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 300
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Current pregnancy or delivery within 6 months
  • Systolic blood pressure > 140 mmHg, or diastolic blood pressure > 90 mmHg at screening
  • BMI > 30 kg/m2
  • Prior history of venous thromboembolism or first degree relatives with history of venous thromboembolism
  • Known predisposition for venous or arterial thromboembolism
  • Prior or ongoing angina pectoris, TIA, myocardial infarction or stroke
  • Myocardial infarction or stroke in first degree relatives
  • Prior reproductive cancer (breast, uterus, cervical)
  • Prior or ongoing pancreatitis
  • Severe and ongoing liver disease or tumor.
  • Migraine with aura
  • Diabetes with known arterial disease
  • Severe dyslipidemia
  • Sensitivity to any of the active components of the investigated product

研究者

发起方
ppsala University

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