跳至主要内容
临床试验/NCT00374634
NCT00374634已完成4 期

Individual Versus Standard rFSH Dose for Controlled Ovarian Stimulation and Intrauterine Insemination. A Prospective Randomised Multi Centre Study

Nina la Cour Freiesleben1 个研究点 分布在 1 个国家目标入组 234 人开始时间: 2006年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
234
试验地点
1
主要终点
Number of mature follicles in the study and control group.

研究概览

简要总结

The purpose of this study is to test if recombinant follicle stimulating hormone (rFSH) given in individual doses, according to a nomogram we have constructed based on our results from a previous study, results in more patients maturing 2-3 follicles compared to standard dose.

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
25 Years 至 39 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Age between 25-39 years
  • First stimulation with rFSH only
  • Indication for intrauterine insemination with standard rFSH starting dose
  • Regular menstrual bleeding with a cycle between 21-35 days
  • Two ovaries
  • Bilateral tuba patency
  • Semen analysis must be sufficient for insemination according to the diagnostic analysis.

排除标准

  • More than three former stimulated intrauterine insemination cycles

研究组 & 干预措施

"Individual" or "standard" rFSH dose

Active Comparator

Patients were randomized to recieve "individual" (50, 75 or 100 IU/day) or "standard" (75 IU/day) rFSh dose. The individual dose was prescribed according to a dosage nomogram based on the patient's body weight (kg) and the total antral follicle count (Freiesleben NC et al., RBMOnline 2009;17:632-64).

干预措施: rFSH drug dose (Drug)

"Standard" rFSH dose

Active Comparator

"Standard" dose of rFSH

干预措施: "Standard" rFSH dose (Drug)

结局指标

主要结局

Number of mature follicles in the study and control group.

次要结局

  • Number of cycles where the rFSH dose is changed.
  • Number of cycles cancelled or converted to in vitro fertilisation.
  • Pregnancy rate.(October 2008)

研究者

发起方
Nina la Cour Freiesleben
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Nina la Cour Freiesleben

MD PhD

Rigshospitalet, Denmark

研究点 (1)

Loading locations...

相似试验