Embryo Selection by Noninvasive Preimplantation Genetic Test

NCT04339166 — Not applicable, Completed, 1152 participants, Peking University Third Hospital

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

RegistryNCT04339166, acronym ESNi-PGT
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: double, screening
Enrollment1152 (Actual)
SponsorPeking University Third Hospital (Other); collaborators: Jinling Hospital, China, Reproductive Medical Center of Hebei Maternity Hospital, Northwest Women's and Children's Hospital, Xi'an, Shaanxi, First Affiliated Hospital of the Chinese People's Liberation Army Naval Medical University, Shengjing Hospital, First Affiliated Hospital, Sun Yat-Sen University, Reproductive & Genetic Hospital of CITIC-Xiangya, Yikon Genomics Company, Ltd, Peking University Shenzhen Hospital, The Second Hospital of Hebei Medical University, West China Second University Hospital, Second Affiliated Hospital of Wenzhou Medical University, Third Affiliated Hospital of Zhengzhou University
ConditionsInfertility, Chromosome Abnormality
InterventionsNon-invasive chromosome screening(NICS) (Diagnostic test)
Datesstart 2020-04-16, primary completion 2024-02-28, completion 2024-08-06, first posted 2020-04-09, last updated 2025-12-11
Locations13 sites in China

Related Papers Related Patents Related Grants Related Experts
All trials for Infertility All trials for Chromosome Abnormality All trials of Non-invasive chromosome screening(NICS)

-Summary

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.

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+Detailed description

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

+Arms and interventions

ArmTypeInterventionsDescription
Group AExperimentalDiagnostic Test: Non-invasive chromosome screening(NICS)Single thawed blastocyst transfer with blastocyst selection according to the analysis of NICS and morphologic score.
Group BNo interventionSingle thawed blastocyst transfer with blastocyst selection according to morphologic score.
  • Non-invasive chromosome screening(NICS) (Diagnostic test): NICS is noninvasive chromosome screening approach to analysis the euploidy by free DNA in embryo culture medium

+Outcome measures

Primary outcomes

  • Ongoing pregnancy rate [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

Secondary outcomes

  • Clinical pregnancy rate [7 weeks after the first embryo transfer]: Number of women with clinical pregnancies after the first transfer / number of women randomized to the specific group
  • Miscarriage rate [Miscarriage:28 weeks of after the first embryo transfer; First trimester miscarriage(early miscarriage):12 weeks of after the first embryo transfer;]: Number of pregnancy losses / number of clinical pregnancies after the first transfer.
  • Live birth rate [within 2 weeks after live birth]: Number of women with live births after the first transfer / number of women randomized to the specific group.

+Eligibility

Sex: Female, ages: 35 Years to 42 Years, accepts healthy volunteers

Inclusion Criteria:

1. Infertile couples receiving IVF- ICSI procedure for assisted reproduction cycle
2. Female age: 35 - 42 years old
3. 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/m2.
4. Culture embryos to blastocyst stage and all the blastocysts will be single cryopreserved.
5. Single frozen-thawed blastocyst Transferred for the first time
6. The number of blastocysts ≥2, morphology grade (above 4BC/4CB)
7. Written informed consent

Exclusion Criteria:

1. 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.)
2. PGT cycles
3. 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
4. Untreated hyperprolactinemia, thyroid disease, adrenal disease
5. Women with endometrial polyps that were not treated before embryo transfer

+Locations (13)

FacilityCityCountryStatus
The First Affiliated Hospital,Sun Yat-sen UniversityGuanzhou, GuangdongChina
Peking University Shenzhen HospitalShenzhen, GuangdongChina
Hebei Maternity and Reproductive hospitalShijiazhuang, HebeiChina
The Second Hospital of Hebei Medical UniversityShijiazhuang, HebeiChina
The Third Affiliated Hospital of Zhengzhou UniversityZhengzhou, HenanChina
Reproductive & Genetic Hospital of Citic-XiangyaChangsha, HunanChina
Jinling Hospital,Nanjing University,School MedicineNanjing, JiangsuChina
Shengjing Hospital of China Medical UniversityShenyang, LiaoningChina
West China Second Hospital of Sichuan UniversityChengdu, SichuanChina
The Second Affiliated Hospital of Wenzhou Medical UniversityWenzhou, ZhejiangChina
Peking University Third HospitalBeijingChina
The First Medical Center of Chinese People's Liberation Army General HospitalBeijingChina
Northwest women's and children's hospitalXi'anChina

+Publications

  • Results publication: Huang J, Li R, Zeng L, Hu L, Cai L, Chen L, Shi J, Wang Y, Guan Y, Xu Y, Qian W, Wang X, Xi H, Zhao Z, Yao Y, Lu S, Yao Y, Wang J, Liu P, Qiao J. Embryo selection by non-invasive preimplantation genetic testing for aneuploidy in women of advanced maternal age: a randomized, clinical trial. Nat Commun. 2026 Sep 8;17(1):10634. doi: 10.1038/s41467-026-77628-4. PMID 42850238
  • Results publication: Huang J, Rong L, Zeng L, Hu L, Shi J, Cai L, Yao B, Wang XX, Xu Y, Yao Y, Wang Y, Zhao J, Guan Y, Qian W, Hao G, Lu S, Liu P, Qiao J. Embryo selection through non-invasive preimplantation genetic testing with cell-free DNA in spent culture media: a protocol for a multicentre, double-blind, randomised controlled trial. BMJ Open. 2022 Jul 27;12(7):e057254. doi: 10.1136/bmjopen-2021-057254. PMID 35896299

+Investigators

  • Jie Qiao, Principal investigator, Peking University Third Hospital