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临床试验/IRCT20200905048630N5
IRCT20200905048630N5尚未招募3 期

Investigating the effect of intraovarian administration of platelet rich plasma in patients with poor ovarian response in improving the result of assisted procedures

Bandare-abbas University of Medical Sciences0 个研究点目标入组 88 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
88

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 45 years(—)
性别
Female

入选标准

  • Informed consent of the patient (completion of the patient consent form by the patient or the patient's companion)
  • Patients aged 18 to 45 years.
  • Patients who have no history of ovarian surgery or ovarian endometrioma.
  • Normal sperm analysis
  • POR (age over 40 years and/or a history of poor response to high-dose stimulation with less than three oocytes and/or adverse ovarian reserve tests including AMH < 1.1 ng/nl; AFC < 7)
  • Patients without endocrine disorders such as hyperprolactinemia, PCOS, etc.
  • Non-smoking patients
  • Patients who do not have cardiovascular disorders.

排除标准

  • Adhesion or severe damage to the pelvis or ovaries
  • Immunological diseases
  • Hematological diseases
  • Platelets less than one hundred and fifty thousand per cubic millimeter
  • Systemic use of corticosteroids within two weeks before the procedure
  • Taking anticoagulants

研究者

发起方
Bandare-abbas University of Medical Sciences

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