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临床试验/NCT05308342
NCT05308342Unknown不适用

Clinical Study of Human Umbilical Cord Mesenchymal Stem Cells in the Treatment of Premature Ovarian Insufficiency

Li-jun Ding1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2019年11月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
66
试验地点
1
主要终点
Follicular development rate

研究概览

简要总结

This study was a single-center, randomized, controlled prospective study. Those who had premature ovarian failure and who had fertility requirements were enrolled in the study. To determine the efficacy and safety of umbilical cord mesenchymal stem cells in the treatment of patients with POI.

详细描述

According to the enrollment and exclusion criteria, the patients were enrolled, and the subjects were randomly divided into two groups by computer randomization. Group A was hormone replacement combined with transplantation of umbilical cord mesenchymal stem cells (test group). Group B was the hormone replacement group (control group).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
20 Years 至 39 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Those who meet the POF diagnostic criteria and have no spontaneous follicular activity;
  • Married, 20 years old ≤ age < 40 years old;
  • The average diameter of each ovary is > 10 mm;
  • Have agreed to sign the informed consent form.

排除标准

  • Female and/or male chromosomal abnormalities;
  • Endometriosis, adenomyosis;
  • Postoperative ovarian borderline or malignant tumor;
  • Uterine dysplasia;
  • Associated with female autoimmune disease or other serious internal surgical diseases;
  • hormone replacement contraindications;
  • In the past 1 year, had received an experimental study of premature ovarian failure in the external hospital;
  • Male azoospermia or severe oligozoospermia.

研究组 & 干预措施

UC-MSCs+hormone replacement group

Experimental

Group A was the hormone replacement combined with transplantation of umbilical cord mesenchymal stem cells group(test group).

干预措施: transplantation of human UC-MSCs into ovaries of POI patients (Procedure)

UC-MSCs+hormone replacement group

Experimental

Group A was the hormone replacement combined with transplantation of umbilical cord mesenchymal stem cells group(test group).

干预措施: hormone replacement treatment (Drug)

hormone replacement group

Active Comparator

Group B was the hormone replacement group (control group).

干预措施: hormone replacement treatment (Drug)

结局指标

主要结局

Follicular development rate

时间窗: 9-12 months

Follicular development and hormonal examination were performed 1 week before treatment and at 1, 2, and 3 weeks after treatment to evaluate the development of follicles. If there is no follicular development in the third week, stop the drug after 1 week, and contact the next treatment time after menstruation. During the follow-up period to half a year after the end of the last treatment, the follicular development activity rate was observed.

次要结局

  • Changes in blood flow index in the ovary(9-12 months)
  • Clinical pregnancy rate(9-12 months)

研究者

发起方
Li-jun Ding
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Li-jun Ding

principal investigator

Nanjing University

研究点 (1)

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