Impact of Storage Time in Liquid Nitrogen on Cryopreserved Human Spermatozoa
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 101
- 试验地点
- 1
- 主要终点
- To evaluate and compare the total and progressive mobility of human spermatozoa post-freezing and post-storage in High Security straws.
研究概览
简要总结
Sperm cryopreservation is an essential tool for men fertility preservation in the context of gonadotoxic treatments or/and pathologies such as cancers, gamete donation and ART. Nevertheless, it is validated that the freezing and thawing procedures affect sperm parameters and in particular motility. It is therefore essential to determine the impact of storage time on motility and particularly the number of progressive motile spermatozoa which will determine the choice of ART technique. However, few studies have analyzed the impact of storage time in liquid nitrogen and no study over a long period on human spermatozoa and their use in ART.
The aim of this study is to assess the impact of long-time storage, from 2 to 12 years, in liquid nitrogen on standard semen parameters, notably motility.
详细描述
It has been demonstrated in the literature that cryopreservation of semen samples in liquid nitrogen guaranty good post thawing motility recovery. However, the literature is scarce and relatively old. Moreover, studies only described very small samples cohort and do not specify in which container the samples are stored. There are currently no published studies on high security straws which are widely used for semen cryopreservation worldwide.
The aim of this study is to assess the impact of long-time storage, from 2 to 12 years, in high security straws, in liquid nitrogen on human standard semen parameters, notably on motility.
Hundred and one cryopreserved semen samples between 2010 to 2020 were donated to research by patients monitored in the unit of Assisted Reproductive Technology - Conservation of human sperm and eggs (ART-CECOS) Unit of the University Hospital of Clermont-Ferrand for fertility preservation. Only samples corresponding to the inclusion criteria below were included in the study without distinction of bio clinical criteria.
All analyzed samples have been cryopreserved following the same protocol, in high security 0,3ml straws, with the same cryoprotectant and using the same programmable freezer Nanodigitcool (CryoBiosystem).
The day of cryopreservation, a post-freezing test (T0) was caried by thawing a straw and by assessing sperm count, motility and vitality according to WHO guidelines 2010.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 19 Years 至 63 Years（Adult）
- 性别
- Male
- 接受健康志愿者
- 否
入选标准
- •The ejaculates were frozen in high security straws by slow freezing,
- •At least two straws per sample were available
- •The "post-freezing" thawing test was carried out on the day of freezing
- •The "post-freezing" thawing test carried out at T0 includes cell numbering, vitality and mobility
- •There is the informed signature of the consent to donate the straws to Research by the patient
排除标准
- •Ejaculate not donated to research, lack of consent to donation to research
- •Frozen ejaculate in microdrop
- •Thawing test not carried out or incomplete
结局指标
主要结局
To evaluate and compare the total and progressive mobility of human spermatozoa post-freezing and post-storage in High Security straws.
时间窗: 07/2022 to 03/2023
The percentage of total and progressive motile human spermatozoa were assessed according to WHO, 2010 guideline.
次要结局
- To compare the number of motile, total and progressive spermatozoa post-freezing and post-storage(07/2022 to 03/2023)
- To compare the vitality of post-freezing and post-storage human spermatozoa(07/2022 to 03/2023)