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临床试验/EUCTR2018-004400-19-ES
EUCTR2018-004400-19-ES进行中(未招募)1 期

Study of the effects of telomerase reactivation with Danazol on ovarian function. A Pilot Study. - Improve fertility in women with low ovarian reserve

IVIRMA MADRID0 个研究点目标入组 45 人开始时间: 2019年4月12日最近更新:
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
45

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

  • -Provide signed and dated informed consent form.
  • -Willing to comply with all study procedures and be available for the duration of the study. This include the decision to use contraception methods different to sexual hormones, such as the use of condoms, during the treatment with Danazol.
  • -female, aged 30 to 45 years old.
  • -In good general health as evidenced by medical history or diagnosed with body mass index between 18 and 30Kg/m2.
  • -Women with normal (AMH value must be equal or higher than 2ng/ml) or compromised ovarian reserve (defined as AMH <2ng/ml).
  • -Not having had any steroid hormones for one month.
  • 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 45
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • -Pregnancy or lactation.
  • -Taking other sexual hormones.
  • -Women with diseases in heart, liver or kidney or tumors which depend on male sexual hormones or hormone-dependent tumour.
  • -Women taking anticonvulsants, medicaments for diabetes, anticoagulants and anti-hypertension: Ciclosporin and tacrolimus and other steroids and statins.
  • -Women suffering irregular genital bleeding or with thrombus or thromboembolic diseases.
  • -Known allergic reactions to components of the study product (cornstarch and lactose).
  • -Having received ovulation induction drugs within one month before the inclusion in the study.
  • -Anything that would place the individual at increased risk or preclude the individual’s full compliance with or completion of the study.
  • -Simultaneous participation in another clinical trial or previous participation in this study.
  • -Participation in another clinical study 2 months before inclusion in the present study that could affect its objectives

研究者

发起方
IVIRMA MADRID

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