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临床试验/NCT07175571
NCT07175571招募中不适用

Prospective Randomized Sibling-Oocyte Trial Comparing Fertilization and Embryo Development Outcomes Between Intracytoplasmic Sperm Injection (ICSI) and Conventional IVF Using Frozen Donor Sperm

Shady Grove Fertility Reproductive Science Center2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2025年9月15日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
95
试验地点
2
主要终点
Blastulation Rate

研究概览

简要总结

The goal of this clinical trial is to learn whether two different methods of helping eggs and sperm join-intracytoplasmic sperm injection (ICSI) and conventional in vitro fertilization (IVF)-lead to better embryo development when using frozen donor sperm in people who do not have male fertility problems. The main questions it aims to answer are:

Does one method create more usable embryos (blastocysts) than the other?

Is there a difference in how often fertilization does not happen at all?

Do either of the methods lead to better embryo quality or early pregnancy?

Participants will:

Have their eggs divided into two groups. One group will be fertilized using ICSI (where a sperm is injected directly into an egg), and the other using conventional IVF (where eggs are mixed with sperm in a dish).

The fertilization method for each egg will be randomly assigned, with a random process also used to determine the assignment of any extra egg when an odd number is collected.

Continue regular fertility treatment while the study team compares the results of each fertilization method.

This study includes people with non-male factor infertility and uses frozen donor sperm. It hopes to learn whether ICSI, which is often used even when it may not be needed, truly helps improve outcomes compared to conventional IVF in these cases.

详细描述

This is a prospective, randomized sibling-oocyte controlled trial designed to compare fertilization and embryo development outcomes between intracytoplasmic sperm injection (ICSI) and conventional in vitro fertilization (IVF) using cryopreserved donor sperm in non-male factor infertility cycles. Despite widespread use of ICSI in assisted reproductive technology (ART), there is insufficient evidence supporting its routine use in non-male factor indications, especially in cycles utilizing frozen sperm where male factor infertility is not a contributing variable.

The study aims to address ongoing clinical debate and practice variation by evaluating whether ICSI offers meaningful advantages over conventional IVF in this specific context. Previous retrospective and meta-analytic data have suggested that while ICSI may reduce total fertilization failure (TFF), it may not improve-and may even negatively impact-other key clinical outcomes such as blastulation rate, embryo quality, and early pregnancy rates in non-male factor populations. Additionally, concerns about increased pregnancy-related complications with ICSI have been raised.

To reduce inter-patient variability and enhance internal validity, a sibling-oocyte design will be employed, allowing within-patient comparison of insemination methods. Oocytes retrieved from each participant will be randomized to either ICSI or conventional IVF. Randomization will be conducted prior to oocyte retrieval using computer-generated allocation. For patients with an even number of mature oocytes, half will be assigned to each insemination method. For those with an odd number, the extra oocyte will be randomly allocated according to the pre-specified scheme.

The fertilization process will begin shortly after oocyte retrieval. In the conventional IVF arm, mature oocytes will be inseminated using washed frozen-thawed donor sperm at a standard concentration and co-incubated for 16-18 hours. In the ICSI arm, a single motile sperm will be injected directly into each mature oocyte. All oocytes will undergo standard embryological assessment post-insemination, and embryos will be cultured under identical conditions.

The primary endpoint is the blastulation rate, defined as the number of usable blastocysts (meeting lab criteria for cryopreservation or transfer) per number of oocytes inseminated in each arm. Secondary outcomes include:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Female patients undergoing IVF with frozen donor sperm at Shady Grove Fertility Center
  • Normal ovarian reserve (AMH > 1 ng/mL, AFC > 10)
  • Absence of male factor infertility
  • Post-wash parameters: >50% motility, >5mil concentration
  • > 4 oocytes retrieved at time of transvaginal oocyte retrieval

排除标准

  • Donor Sperm with significant male factor infertility (e.g., abnormal sperm concentration, motility, or morphology)
  • Any medical condition contraindicating ART

结局指标

主要结局

Blastulation Rate

时间窗: Day 5 to Day 7 post-insemination

The blastulation rate is defined as the number of "usable" blastocysts divided by the number of oocytes inseminated in each arm (ICSI and conventional IVF). A blastocyst is considered "usable" if it meets laboratory criteria for either cryopreservation or embryo transfer. Assessment is performed on Days 5-7 after fertilization using standard morphological grading under light microscopy.

次要结局

  • Fertilization Rate(Approximately 16-18 hours post-insemination)
  • Total Fertilization Failure (TFF)(Approximately 16-18 hours post-insemination)
  • Proportion of High-Quality Blastocysts(Day 5 to Day 7 post-insemination)
  • Early Clinical Pregnancy Rate(Approximately 5 to 7 weeks after embryo transfer)

研究者

发起方
Shady Grove Fertility Reproductive Science Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Kate Devine

Medical Director and Chief Research Officer

Shady Grove Fertility Reproductive Science Center

研究点 (2)

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