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临床试验/NCT04339166
NCT04339166已完成不适用

A Multicenter Clinical Study on Embryo Selection by Using the Ploidy of Cell Free DNA in Embryo Culture Medium

Peking University Third Hospital25 个研究点 分布在 1 个国家目标入组 1,152 人开始时间: 2020年4月16日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
1,152
试验地点
25
主要终点
Ongoing pregnancy rate

研究概览

简要总结

The objective of this study is to explore whether non-invasive chromosome screening (NICS) can be used as an effective indicator for embryos selection besides morphology through a multicenter randomized controlled trial, by comparing the differences of live birth rate, pregnancy rate and miscarriage rate between the two groups of embryo selection by "NICS+ morphology" and embryo selection only by "morphology" in IVF cycle.

详细描述

Chromosomal abnormalities commonly exist in early human embryos, and often cause embryo implantation failure and pregnancy loss in in-vitro fertilization (IVF) treatments. Preimplantation genetic testing for aneuploidies (PGT-A) by comprehensive chromosome screening (CCS) has been widely applied in IVF practices to select embryos with normal ploidy. Although multiple clinical trials have demonstrated improved clinical outcomes with PGT-A, it's in controversial for whether PGT-A is truly worthwhile to be offered to all IVF patients. One of the main concerns is that it involves an embryo biopsy procedure, which is invasive and the long-term safety issue of the embryo biopsy remains to be fully investigated.

In recent years, researchers have found that the spent medium of embryo culture contains trace amount of cell-free DNA, which may reflect the ploidy of the embryo. The non-invasive chromosome screening (NICS) approach utilizing spent culture medium samples has been evaluated in studies. However, the clinical value of NICS as a new effective indicator to evaluate embryo competence so far has not been justified by randomized clinical trials.

The main purpose of this project is to verify whether NICS can be used as a new effective indicator for evaluating embryo developmental potential through multi-center, randomized clinical trials

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Screening
盲法
Double (Participant, Investigator)

入排标准

年龄范围
35 Years 至 42 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Infertile couples receiving IVF- ICSI procedure for assisted reproduction cycle
  • •Female age: 35 - 42 years old
  • •Women receiving controlled ovarian hyperstimulation treatment (including ultra-long protocol、long-protocol 、short protocol treatment with GnRH agonist and GnRH antagonist treatment protocol); and the number of oocytes ≥6; The female BMI is from 18 to 30kg/m
  • •Culture embryos to blastocyst stage and all the blastocysts will be single cryopreserved.
  • •Single frozen-thawed blastocyst Transferred for the first time
  • •The number of blastocysts ≥2, morphology grade (above 4BC/4CB)
  • •Written informed consent

排除标准

  • •One of couples with IVF or ICSI contraindications(such as poorly controlled type I or type II diabetes; liver disease or dysfunction; kidney disease or renal function abnormality; significant anemia; history of deep venous thrombosis, pulmonary embolus; history of cerebrovascular accident; uncontrolled hypertension or diagnosed heart disease; history of cervical, endometrial or breast cancer; undiagnosed vaginal bleeding.)
  • •Women who have pathologies or malformations that affect the pregnancy outcome: genital malformations, untreated hydrosalpinx, untreated uterine infections, intramural myomas > 4cm , benign tumor of pelvic and abdominal cavity> 4cm, intimal thickness<8mm, pituitary tumors and malignant tumors of various tissues and organs during the patient's participation in the study
  • •Untreated hyperprolactinemia, thyroid disease, adrenal disease
  • •Women with endometrial polyps that were not treated before embryo transfer

研究组 & 干预措施

Group A

Experimental

Single thawed blastocyst transfer with blastocyst selection according to the analysis of NICS and morphologic score.

干预措施: Non-invasive chromosome screening(NICS) (Diagnostic Test)

Group B

No Intervention

Single thawed blastocyst transfer with blastocyst selection according to morphologic score.

结局指标

主要结局

Ongoing pregnancy rate

时间窗: 12 weeks after the first embryo transfer

Number of women with ongoing pregnancies after the first transfer/ number of women randomized to the specific group

次要结局

  • Clinical pregnancy rate(7 weeks after the first embryo transfer)
  • Live birth rate(within 2 weeks after live birth)
  • Clinical pregnancy rate(7 weeks after the first embryo transfer)
  • Miscarriage rate(Miscarriage:28 weeks of after the first embryo transfer; First trimester miscarriage(early miscarriage):12 weeks of after the first embryo transfer;)
  • Live birth rate(within 2 weeks after live birth)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jie Qiao

Professor

Peking University Third Hospital

研究点 (25)

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