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临床试验/NCT03946813
NCT03946813已完成不适用

The Efficacy of Platelets Rich Plasma (PRP) for Ovarian Rejuvenation

Al-Kindy College of Medicine1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2018年8月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
1
主要终点
Anti-Müllerian hormone (AMH) concentration

研究概览

简要总结

In recent years, an increased approach has appeared in the use of autologous blood products to assist tissue and organ healing. Application of platelet rich plasma (PRP) has emerged as a potential solution for infertile women with poor ovarian reserve in reproductive specialty.

详细描述

Quantitative and qualitative functional improvement of ovarian function has been reported in several studies after using autologous PRP in a reproductive field. Ovarian rejuvenation, stimulating the ovaries to produce new eggs after injecting PRP, can offer hope for renewed fertility to women with poor reserve volume, advanced maternal age, or either naturally occurring or premature menopause. But, these encouraging results should be supported by several new studies.

This study aimed to estimate the efficacy of trans-vaginal ovarian injection with PRP in rejuvenates ovaries in woman with poor ovarian reserve, and to assess any association of some women variables (age, menstrual status, parity, BMI) as predicting factors in success of ovarian injection with PRP.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 49 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Menopause or peri-menopause under the age of
  • Premature ovarian insufficiency which is ovarian failure before the age of
  • Woman with primary ovarian failure of any cause.

排除标准

  • A previous injection with any medication, plasma, or PRP
  • Invisible or difficult access ovaries.
  • Medical disease or unfit for anesthesia patient.

结局指标

主要结局

Anti-Müllerian hormone (AMH) concentration

时间窗: 4 weeks

Before after intervention measurement

Follicle-stimulating hormone (FSH) concentration

时间窗: 4 weeks

Before after intervention measurement

Antral follicles numbers

时间窗: 4 weeks

Before after intervention measurement

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yousif Abdulraheem

Professor

Al-Kindy College of Medicine

研究点 (1)

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