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临床试验/CTRI/2022/09/045274
CTRI/2022/09/045274已完成未知

Efficacy of flexible Progestin primed ovarian stimulation(f-PPOS) protocol comapred to flexible GnRH antagonist protocol for assisted reproductive technology in voluntary oocyte donors- a randomized trial

Indira IVF Hospital Pvt Ltd0 个研究点目标入组 91 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
91

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

入选标准

  • 1)All voluntary egg donors giving consent to participate in the study.
  • 2) Age 21 to 35 yrs.
  • 3) Having at least one healthy living child.
  • 4) AFC 10 to 25

排除标准

  • 1)Poor ovarian reserve defined as antral follicle count (AFC) < 5
  • 2) BMI >30 kg/m2
  • 3) Having following gynaecological conditions like ovarian endometriosis, Oestrogen dependent tumour like endometrial or breast carcinoma.
  • 4) Received luteal phase GnRH agonist use for suppression
  • 5) Uncontrolled diabetes, hypertension or thyroid disorder
  • 6) Diagnosed to be sero-positive for HIV, HBSAg, or HCV
  • 7) Active infection of Covid 19 by RT-PCR
  • 8) Known genetic or hereditary disease in herself or her child
  • 9) Diagnosed haemoglobinopathy like Thalassemia or Sickle cell disease.
  • 10) Any follicle measuring =9 mm on D2/ D3 scan.

研究者

发起方
Indira IVF Hospital Pvt Ltd

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