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临床试验/NCT05017740
NCT05017740进行中(未招募)不适用

A Randomised Clinical Trial in the Use of Physiological Intra-cytoplasmic Spermatozoa Injection (PICSI) in Couples With a Previous Poor Fertilisation Cycle in In-vitro Fertilisation.

KK Women's and Children's Hospital1 个研究点 分布在 1 个国家目标入组 47 人开始时间: 2022年3月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
47
试验地点
1
主要终点
Clinical pregnancy rate

研究概览

简要总结

Poor fertilisation plays a significant role in poor artificial reproductive technique outcomes. Male factor infertility accounts for a large portion of such cases. Several modalities have been proposed as a solution, including physiological intra-cytoplasmic sperm injection (PICSI). PICSI is a technique used to select the sperm to use in intra-cytoplasmic sperm injection (ICSI) treatment. It involves placing sperm with hyaluronic acid, a natural compound found in the body. PICSI identifies sperm that can bind to hyaluronic acid and these sperms are selected for use in treatment.

Some studies have suggested that PISCI may be advantageous to reduce miscarriage. However, the evidence is not strong and it remains unknown if PICSI is effective in a selected group of couples with a history of poor fertilisation. Based on previous medical records, we observed a higher clinical pregnancy rate (CPR) and a trend towards lower miscarriage rates with PICSI. To verify the findings and address the clinical gap, we propose a randomised controlled trial (RCT) with 234 couples (117 in each group) to evaluate the effectiveness of PICSI comparing with ICSI for improving CPR and reducing miscarriage rate in couples with a fertilisation rate of <50% in their first cycle of ICSI.

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, Outcomes Assessor)

盲法说明

Trial participants, research team collecting data outcome, and all study team members except the embryologists will be blinded to treatment allocation. It is not possible to conceal allocation to the embryologists, who will perform the intervention.

入排标准

年龄范围
21 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Couples with <50% fertilisation in their first ICSI cycle, and scheduled for their second ICSI/PICSI cycle

排除标准

  • •Women with diminished ovarian reserves (AMH <1.2ng/ml) or severe endometriosis (rAFS Stage III or IV)
  • •Male partner with severe oligoasthenoteratozoospermia (Density < 5 million, Total motility < 40) or those require surgically retrieved sperm
  • •Couples using donor gametes
  • •Couples using frozen gametes
  • •Couples undergoing split IVF-ICSI cycles
  • •Couples where a freeze all approach has been done, either clinically indicated or secondary to patient choice

研究组 & 干预措施

ICSI

Active Comparator

干预措施: ICSI (Procedure)

PICSI

Active Comparator

干预措施: PICSI (Procedure)

结局指标

主要结局

Clinical pregnancy rate

时间窗: 6-9 weeks after fresh embryo transfer

The presence of fetal heartbeat or gestational sac at 6-9 weeks after fresh embryo transfer

Miscarriage rate

时间窗: 6 to 23+6 gestational weeks

Pregnancy loss before 23+6 completed weeks after confirmation of clinical pregnancy

次要结局

  • Fertilisation rate(2-5 days after oocyte retrieval)
  • Live birth rate(After 24 completed weeks of gestation)

研究者

发起方
KK Women's and Children's Hospital
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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