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临床试验/NCT01111084
NCT01111084已完成不适用

Prospective Multi-centre Observational Study to Determine the Mono-bifollicular Development in Infertile Women Subjected to Ovulation Induction With Follitropin α

Merck KGaA, Darmstadt, Germany1 个研究点 分布在 1 个国家目标入组 410 人开始时间: 2004年3月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
410
试验地点
1
主要终点
Follicular development

研究概览

简要总结

This is a prospective and multicentric observational study to determine the real mono-bifollicular development rate that is obtained under normal care conditions following ovulation induction (OI) treatment with follitropin-alpha filled by mass prescribed in accordance with standard practice.

详细描述

In women with infertility due to anovulation, the main purpose of ovulation induction (OI) consists in inducing the mono or bifollicular and the subsequent ovulation in order to achieve pregnancy. The availability of recombinant gonadotropins obtained using genetically engineered techniques has meant a decisive and clear pharmacological advancement. Use of recombinant human follicle stimulating hormone (r-hFSH) offers a greater effectiveness (greater number of follicles/ ovocytes and a higher pregnancy rate) and efficiency (fewer number of blisters, fewer stimulation days; fewer number of cancellations and complications) in programmed coitus and artificial insemination like in-vitro fertilisation (IVF)/intra cytoplasmic sperm injection (ICSI) techniques. Further advances in obtaining better products for ovarian stimulation has led to production of a recombinant FSH (follitropin alpha) filled by mass preparation. This hormone becomes the most consistent and precise gonadotropin due to improvements in its quantification process.

Today, despite having accurate and modern tools for ovulation induction, in daily practice, doctors continue to "fight" against two old problems of assisted reproduction: multiple pregnancies and ovarian hyperstimulation syndrome (OHSS). Application of assisted reproduction techniques (ARTs) and the use of medication that induce ovulation, risk producing gestations and multiple births with a higher frequency than those observed in spontaneous gestations. One of the facts that result in the appearance of such problems is the high incidence of polycystic ovarian syndrome among the population of women who are infertile due to anovulation. These subjects are especially sensitive to ovarian stimulation, which leads to multiple follicular development, a higher risk of hyperstimulation and higher rates of multiple pregnancies.

Therefore, it seems clear that the search for developing mono or bifollicular cycles is important in ovarian induction cycles, for the purpose of preventing the above mentioned multiple pregnancy problems and the risk of OHSS. The intent of this study was to figure out the real mono-bifollicular development rate that is obtained under normal care conditions following OI treatment with follitropin alpha filled by mass prescribed in accordance with standard practice. Therefore, a measure of the efficiency of the product for achieving the development of one or two follicles. Data was collected from 56 centres of the Autonomous Communities that accepted this observational study, until achieving a total of 410 ovulation induction cycles.

OBJECTIVES

Primary objective:

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Premenopausal women with infertility caused by anovulation, who wished to conceive and were included in an ovulation induction (OI) treatment protocol for intrauterine insemination or for programmed coitus

排除标准

  • Subjects with hypersensitivity to follitropin alpha, to FSH or to any of the excipients
  • Subjects with hypothalamic or pituitary tumours
  • Subjects with increase in the size of the ovaries or cysts that were not due to polycystic ovary disease
  • Subjects with gynaecologic haemorrhages of unknown aetiology
  • Subjects with ovarian, uterine or mammary carcinoma
  • Subjects with primary ovarian failure
  • Subjects with malformations of sex organs that were not compatible with pregnancy
  • Subjects with uterine fibroid tumours that were not compatible with pregnancy

结局指标

主要结局

Follicular development

时间窗: First 10 months from the inclusion of the subjects

Number and size of follicles as determined through transvaginal ultrasound

次要结局

  • Secondary efficacy assessments(From baseline until the pregnancy or menstruation confirmation)
  • Safety assessments(First 10 months from the inclusion of the subjects)

研究者

申办方类型
Industry

研究点 (1)

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