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临床试验/IRCT2017091736235N1
IRCT2017091736235N1招募中未知

Comparing the outcomes of dual trigger with GnRh agonist along with HCG versus HCG alone in normal responder patients in antagonist ART protocol

Avicenna Research Institute0 个研究点目标入组 164 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
164

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Infertility due to male factor, tubal factor or unexplained; IVF less than 2 times; age between 18 and 40; BMI between 18 and 30; normal PRL and TSH; FSH less than 10; The minimum sperm count, 10 million and the minimum 3% of the sperms should have normal morphology. Exclusion criteria: AFC more than 15; E2 more than 3000 at trigger day or AFC more than 20; sensitization to HCG or gonadotropins; FSH more than 10 at third day of cycles or AFC less than 5; AUB; documented uterine anomaly in hysterogram or HSG; endometriosis (grade 3 and 4); Diabetes or uncontrolled HTN, kidney or liver dysfunction; PCO; Cancer, tumor, or pituitary adenoma; Ovarian cysts; hydrosalpinx; intramural or submucosal myoma larger than 6cm

排除标准

  • 未提供

研究者

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