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A Study on the Effect of Euploid Blastocyst Screening Assisted by Human Euploid Embryo AI Real time Screening Model(AMCFNet) on the Clinical Outcome of IVF-ET/ICSI-ET Treatment in Elderly Infertile Patients——A multicenter, prospective controlled clinical study

A Study on the Effect of Euploid Blastocyst Screening Assisted by Human Euploid Embryo AI Real time Screening Model(AMCFNet) on the Clinical Outcome of IVF-ET/ICSI-ET Treatment in Elderly Infertile Patients——A multicenter, prospective controlled clinical study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069161
Enrollment
Unknown
Registered
2023-03-08
Start date
2023-03-08
Completion date
Unknown
Last updated
2023-05-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

infertility

Interventions

AI assisted embryo screening group ( experimental group ):Artificial intelligence assisted embryo screening
Artificial screening embryo group (Control group):Artificial screening embryo

Sponsors

The First Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 42 Years

Inclusion criteria

Inclusion criteria: 1.Couples with IVF / ICSI indications ,female aged between 35-42 years old and BMI in the range of 18-30kg/m2; 2.Infertile female who underwent the first or second cycle of IVF-ET/ ICSI-ET treatment; 3.Routine controlled ovarian stimulation with long GnRH agonistGnRH antagonist protocol or luteal phase ovarian stimulation; 4.The number of oocytes obtained = 6; 5.Normal fertilized embryos are continuously cultured in time-lapse; 6.All D3 cultured into blastocysts, and D5 / 6 / 7 blastocysts = 2, and the morphological rating was above 4BC / 4CB; 7.Fully informed understanding of this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Infertility patients treated with PGT; 2.Uterine septum, unicornuate uterus, double uterus and other reproductive tract malformations; 3.Intrauterine adhesions, uterine effusion, multiple endometrial polyps, submucous uterine fibroids or thin endometrium ( embryo transfer day endometrial thickness < 7mm ); 4.Patients with hydrosalpinx who were not treated with tubal ligation or blockage; 5.Patients with a history of autoimmune or endocrine diseases : systemic lupus erythematosus ( SLE ), undiferentiated connective tissue disease( anti-ANA positive ), hyperthyroidism, hypothyroidism, etc. 6.Recurrent implantation failure(no pregnancy after 3 or more high quality embryo transfer)or unexplained early pregnancy loss at least twice; 7.At least one of the couples has IVF or ICSI contraindications ( such as poorly controlled type I or type II diabetes unexplained liver disease or liver dysfunctionrenal disease or renal dysfunctionsevere anemiahistory of deep vein thrombosis, pulmonary embolism, cerebrovascular accidentpoorly controlled hypertension or diagnosed heart diseasehistory of cervical cancer, endometrial cancer or breast cancerunexplained vaginal bleeding, etc ).

Design outcomes

Primary

MeasureTime frame
ongoing pregnancy rate;

Secondary

MeasureTime frame
live birth rate;miscarriage rate;clinical pregnancy rate;

Countries

China

Contacts

Public ContactQingyun Mai

The First Affiliated Hospital of Sun Yat-sen University

maiqy@mail.sysu.edu.cn13724013011

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026