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临床试验/NCT01752270
NCT01752270Unknown4 期

The Effect of Diane-35 Pretreatment on Endocrine and Clinical Profile for Patients With Polycystic Ovary Syndrome Undergoing In-vitro Fertilization

First Affiliated Hospital, Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2012年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
100
试验地点
1
主要终点
fertilization rate

研究概览

简要总结

Polycystic Ovary Syndrome is the most common endocrine disorder in women, is estimated to affect more than 5% of the population and is associated with chronically elevated serum androgen concentrations.Evidence suggests that polycystic ovary syndrome has a negative impact on pregnancy outcomes, with an increased risk of gestational diabetes, hypertensive disease during pregnancy,and preterm birth,which is partially related with the hyperandrogenic environment.Diane-35 has been proved to be the most effective anti-androgenic drug.At present, there is no direct evidence that Diane-35 has a positive effect on the clinical outcome of polycystic ovary syndrome patients undergoing In-vitro fertilization/Intracytoplasmic sperm injection.

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
20 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • diagnosed polycystic ovary syndrome patients according to Rotterdam criteria
  • with hyperandrogenism and/or clinical hyperandrogenic manifestations
  • no other oral contraceptives treatment for at least 3 months before this experiment
  • no any other assisted reproductive therapy
  • accompanied with fallopian tube and/or male factors
  • normal hepato-/nephro- function

排除标准

  • oral contraceptive pills contraindications, eg.Deep Venous Thrombosis
  • smoking, drunk
  • exclude other infertile factors, eg.endometriosis, abnormal thyroid function, etc.

研究组 & 干预措施

diane-35

Experimental

Diane-35 pretreatment from the third day of menstrual cycle

干预措施: Diane-35 pretreatment (Drug)

结局指标

主要结局

fertilization rate

时间窗: up to 2years

次要结局

  • implantation rate(up to 2years)

研究者

发起方
First Affiliated Hospital, Sun Yat-Sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhou Canquan

vice president

First Affiliated Hospital, Sun Yat-Sen University

研究点 (1)

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