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临床试验/NCT00915915
NCT00915915已完成2 期

Multicenter, Open-label, Randomized Study to Evaluate Inhibition of Ovulation of Two Transdermal Patch Formulations Containing 0.55 mg Ethinylestradiol and Either 1.05 or 2.1 mg Gestodene in Healthy Young Female Volunteers Over a Period of 3 Treatment Cycles

Bayer0 个研究点目标入组 108 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Bayer
入组人数
108
主要终点
The primary efficacy variable will be the proportion of volunteers with ovulation in at least one of the treatment cycles 2 and 3

研究概览

简要总结

Investigation of two transdermal hormone patch formulations for contraception regarding inhibition of ovulation over a period of 3 treatment cycles in healthy young female volunteers

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • BMI: 18 BMI 30 kg/m²
  • Healthy female volunteers
  • Age 18-35 years (smoker not older than 30 years, inclusive)
  • Ovulatory pre-treatment cycle, at least 3 month since delivery
  • Abortion or lactation before the first screening examination
  • Willingness to use non-hormonal methods of contraception during entire study

排除标准

  • Contraindications for use of combined (estrogen/gestodene) contraceptive (e.g. history of venous/artial thromboembolic disease
  • Regular intake of medication other than OCs
  • Clinically relevant findings (blood pressure, physical and gynaecological examination, laboratory examination) anovulatory pre-treatment cycle

研究组 & 干预措施

Arm 1

Experimental

干预措施: Ethinylestradiol/Gestodene (BAY86-5016) (Drug)

Arm 2

Experimental

干预措施: Ethinylestradiol/Gestodene (BAY86-5016) (Drug)

结局指标

主要结局

The primary efficacy variable will be the proportion of volunteers with ovulation in at least one of the treatment cycles 2 and 3

时间窗: 4 months

次要结局

  • The primary efficacy variable will be the proportion of volunteers with ovulation in at least one of the treatment cycles 2 and 3(4 months)
  • Pharmacokinetics of Ethinylestradiol (EE), Gestodene (GSD) and SHBG in treatment cycles 2 and 3(4 Months)
  • Cervical effects (Insler Score) for determination of hormonal effects on the cervix and the cervical mucus during pre-treatment cycle and treatment cycle 3(4 Months)
  • Course of gonadotropins (FSH, LH, P, E2)(4 months)
  • Endometrial thickness and Follicle size(4 months)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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