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Evaluation Of Endometrial Receptivity By Artificial Intelligence Based On Ultrasound Radiomics

Evaluation Of Endometrial Receptivity By Artificial Intelligence Based On Ultrasound Radiomics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126067
Enrollment
Unknown
Registered
2026-06-03
Start date
2023-10-31
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

infertility

Interventions

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the repetitive study: 1.Women with a history of pregnancy or childbirth (including delivery, induced abortion, medical abortion, and spontaneous abortion, but excluding ectopic pregnancy); 2.Regular menstrual cycles of 28–35 days; 3.Age between 20 and 40 years. Inclusion Criteria for Ultrasound Radiomics Prediction of Endometrial Receptivity: 1. Infertile patients undergoing IVF-ET/ICSI-ET 2. with standard luteal phase long protocol, follicular phase long protocol, GnRH-a prolonged protocol or antagonist protocol, and at least have one high-quality embryo for transfer 3. In frozen-thawed embryo transfer cycle, endometrial preparation include natural cycle, ovulation induction cycle, HRT cycle or GnRHa-HRT cycle, and at least have one high-quality embryo for transfer 4. Age 20-40.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for the repetitive study: 1. Acute stage of pelvic inflammatory disease; 2. Recent or ongoing hormone therapy; 3. History of recurrent spontaneous abortion (=2 pregnancy losses before 28 weeks of gestation with the same partner); 4. Conditions that may affect endometrial receptivity (uterine malformations, intrauterine adhesions, thin endometrium (endometrial thickness <7 mm), endometriosis, adenomyosis, endometrial polyps, submucosal fibroids, hydrosalpinx, etc.); 5. Presence of an intrauterine contraceptive device; 6. Lactation period; 7. Luteinized unruptured follicle syndrome (cycles with luteinization will be cancelled; participants may re-enter the study in the next cycle. Participants will be excluded if luteinization occurs consecutively); 8. Failure to complete two cycles of sample collection (e.g., pregnancy after the first cycle or voluntary withdrawal during the study). Exclusion Criteria for Ultrasound Radiomics Prediction of Endometrial Receptivity: 1. Chromosomal abnormalities in one or both spouses leading to abortion 2. Recurrent miscarriage (=2 pregnancies with the same spouse before 28 weeks) 3. Abnormal uterine cavity (uterine malformation, history of intrauterine adhesions, endometrial polyps, submucosal uterine fibroids, endometrial dysplasia, etc.) 4. Endometriosis disease (including uterine glandular myopathy) 5. Untreated hydrosalpinx 6. Autoimmune diseases and prethrombotic state 7. Failure to complete ultrasound measurement, or incomplete follow-up data in medical records. 8. Failure to complete the embryo transfer in the cycle.

Design outcomes

Primary

MeasureTime frame
Embryo Implantation Rate;Clinical Pregnancy Rate;Miscarriage Rate;Live Birth Rate;

Countries

China

Contacts

Public ContactYihua Yang

The First Affiliated Hospital of Guangxi Medical University

workyyh@163.com+86 150 0773 7358

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026