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临床试验/NCT00650754
NCT00650754终止2 期

A Randomized Double Blinded Trail of DHEA Supplementation for Treatment of Couples With Normal Hysterosalpingogram and Normal Semen Analysis and Evidence of Premature Ovarian Aging (POA).

Center for Human Reproduction1 个研究点 分布在 1 个国家目标入组 35 人开始时间: 2008年3月最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
35
试验地点
1
主要终点
Live Birth

研究概览

简要总结

The experimental focus of this project is on the interaction of DHEA treatment on pregnancy in women with otherwise unexplained infertility and evidence of premature ovarian aging (POA).

详细描述

Recruitment:

Eligible patients will be recruited by advertising on the web and in newspaper. We will screen women under 38 years old with regular menstrual cycles and more than one year of infertility.

Experimental plan:

  1. Informed consent
  2. Baseline studies
  • Antral follicle counts on Day 2 - 3 of cycle
  • Day 3 Serum FSH, LH, E2, Prog, DHEA, DHEAS, testosterone, AMH, Fragile X
  1. Randomization for pretreatment

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
21 Years 至 37 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • >= 1 year of infertility
  • < 38 years old
  • Normal HSG
  • Normal Semen analysis (Count >= 20 million/ motility > 50%/ Kruger morph > 14%.
  • Regular menses
  • Willingness to sign informed consent for study randomization
  • Willingness to participate in 8 months of non-IVF will he him treatment.

排除标准

  • Abnormal semen analysis
  • Abnormal HSG
  • Baseline FSH/E2 within normal age specific criteria
  • Medical condition that would contraindicate pregnancy, ovulation induction or general anesthesia
  • Family history of significant genetic disease, or factor V leiden thrombophilia
  • Inability to present for monitoring visits
  • Inability to follow medication instruction
  • Desire to undergo other fertility treatments before completing eight months of this trial

结局指标

主要结局

Live Birth

时间窗: 24 months

次要结局

  • Androgen side effects(12 months)
  • Endocrine effects(12 months)
  • Clinical Pregnancy(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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