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临床试验/NCT06117982
NCT06117982已完成2 期

Does Subcutaneous Granulocyte Colony Stimulating Factor (G-CSF) Improve Ovarian Reserve in Women With Premature Ovarian Insufficiency?

Trio Fertility2 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2023年10月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
11
试验地点
2
主要终点
Improving ovarian reserve markers

研究概览

简要总结

The goal of this pilot study is to improve ovarian reserve markers in patients with premature ovarian insufficiency. The main question it aims to answer is:

- Will treatment with G-CSF allow improvement in markers of ovarian reserve?

详细描述

The research team hypothesize that treatment of premature ovarian insufficiency patients with G-CSF to mobilize bone marrow hematopoietic stem cells will allow for improved ovarian reserve markers including antral follicle count, anti-Mullerian hormone (AMH) levels and gonadotropin (FSH) levels. The research team anticipate these outcomes:

  • Primary outcome: Decreased serum FSH and increased AMH levels and u/s measurement of increased antral follicle count (AFC)
  • Secondary outcome: Improved ovarian response in IVF cycles if BAFs develop, and spontaneous or IVF pregnancy.

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
25 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women ages 25-40
  • Woman who meet criteria for POI defined as AFC < 5, AMH < 3 pmol/L and FSH >30 IU/L. There may also be associated symptoms of the menopause such as hot flushes, night sweats, insomnia and vaginal dryness.
  • Women who are not taking any other medical or fertility treatments except natural estrogen to stop hot flushes.
  • Those who are provided with informed consent.

排除标准

  • Women with age > 40
  • Women with history of autoimmune disorders
  • Women with a history of hematopoietic cell malignancies
  • Women with sickle cell disease
  • Women with any other comorbidities that would preclude infertility treatment and pregnancy such as HIV/AIDS, hepatitis B or C, breast cancer or body mass index (BMI) >40.

研究组 & 干预措施

Patients with POI receiving G-CSF injections

Experimental

Patients will receive 0.5 ml SC injections of G-CSF (Neupogen, Amgen, USA) at 300 micrograms/day for 4 consecutive days. The first injection will be administered in our office with a 60-minute observation period. Subsequent injections can be self-administered at home for three days, with a return to our clinic for monitoring the following day. This 4-day Neupogen regimen will be repeated in one month.

Patients may undergo two rounds of G-CSF treatment one month apart. If no improvement is observed in gonadotropin, anti-Mullerian levels, and antral follicle count, a third treatment may be offered a month later. Follow-up includes blood assessment of AMH and FSH, as well as ultrasound measurement of basal antral follicle count for three months after the last G-CSF infusion.

干预措施: Neupogen (Drug)

结局指标

主要结局

Improving ovarian reserve markers

时间窗: It is anticipated within six months

Success of the treatment will be assessed by a change in serum FSH, AMH (measure of ovarian reserve) and number of antral follicles (AFC).

FSH Level (IU/L)

时间窗: Baseline to Month 12

Success of the treatment will be assessed by a change in serum FSH, AMH (measure of ovarian reserve) and number of antral follicles (AFC).

AMH Level (Pmol/L)

时间窗: Baseline to Month 12

AMH level for ovarian reserve

次要结局

  • Successful Pregnancy(It is anticipated after the first six months of the study time frame)
  • Successful Pregnancy(From Baseline to Month 12)

研究者

发起方
Trio Fertility
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Robert F. Casper

Scientific Director, MD, FRCSC, REI

Trio Fertility

研究点 (2)

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