跳至主要内容
临床试验/IRCT201312251141N16
IRCT201312251141N16已完成4 期

Compare the efficacy of two protocols of ovarian stimulation using Gonal-F and Luveris in women with hypogonadotropic hypogonadism undergoing assisted reproductive technique Compare the efficacy of two protocols of ovarian stimulation using Gonal-F and Luveris in women with hypogonadotropic hypogonadism undergoing assisted reproductive technique

Royan Institute0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
no limit 至 no limit(—)
性别
Female

入选标准

  • Inclusion Criteria:
  • Have a clinical history of hypogonadotropic hypogonadism, and laboratory test result comply with diagnosis of hypogonadotropic hypogonadism; Have discontinued gonadotropins or gonadotropin releasing hormone or estrogen-progesterone replacement therapy at least one month before the study; Have primary or secondary amenorrhea; Serum LH and FSH <5.0 IU/l and oestradiol <100 pg/ml before initiation of treatment; Have a negative progesterone challenge test; Normal serum concentrations of thyroid stimulating hormone (TSH), prolactin and testosterone within 6 months before the start of study; Have given written informed consent prior to any study related procedure

排除标准

  • The other causes of infertility; History of ovarian hyper stimulation syndrome; Abnormal gynecological bleeding of undetermined origin; Previous or current hormone dependent tumor

研究者

相似试验