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Construction of CITIC Xiangya Assisted Reproduction Data Repository

CITIC Xiangya Assisted Reproduction Data Repository: a Real Medical Environment Based Research Database

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05404464
Acronym
CXARDR
Enrollment
119590
Registered
2022-06-03
Start date
2016-01-01
Completion date
2023-06-30
Last updated
2022-06-03

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

Conditions

Assisted Reproductive Technology, Infertility

Keywords

Population-based database, Registry, Infertile couple and offspring, Longitudinal study

Brief summary

Human Assisted Reproductive Technology (ART) has become a very effective and nearly irreplaceable clinical treatment for infertility, helping millions of women achieve fertility. However, ART may still have potential health risks to mothers and offspring. To better research and monitor the efficacy and safety of ART, the investigators established CXARDR based on the real medical data in Reproductive and Genetic Hospital of CITIC-Xiangya, which is the world's largest ART single treatment center. CXARDR covers the ART full-cycle treatment records since the hospital perfected its electronic medical record system in 2016, as well as biological samples from the CITIC-Xiangya Genetic Resource Bank. From the preoperative investigation of ART to the 1-year follow-up of ART offspring, CXARDR provides the details of the whole process of treatment and the follow-up outcomes of ART patients, making up for the gap in the data of reproductive and obstetric institutions. The huge biological samples with clinical information also provide more possibilities for in-depth basic researches in the field of reproduction and genetics. During the past five years (January 2016 to November 2020), the CXARDR has accumulated data concerning more than 223,000 ART treatment cycles from 120,000 infertile couples. The CXARDR also links more than 180,000 blood samples, 65,000 follicular fluid samples, 80,000 semen samples, and 31,000 granulosa cell samples from 75,000 couples. The data volume is substantial with over 800 variables being documented, and most variables are designed as structured fields. The whole process of data access, data extraction, data processing and data analysis was conducted through a dedicated server inside the CITIC-Xiangya Data Center. All investigators cannot access sensitive information, are required to sign data confidentiality agreement, and need to be approved by the CITIC-Xiangya Ethics Committee.

Interventions

OTHERDifferent baseline characteristics and clinical management

Personal history, basic diseases, stimulation plan, type of ART, transplantation strategy, etc.

Sponsors

Central South University
CollaboratorOTHER
West China Hospital
CollaboratorOTHER
Reproductive & Genetic Hospital of CITIC-Xiangya
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 66 Years
Healthy volunteers
No

Inclusion criteria

* All infertile couples undergoing ART treatment in our hospital (CITIC-Xiangya) were enrolled.

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Weight of offspring 1 year oldUp to 1 year after deliverySelf-measurement
Cleavage rateUp to 3 days after inseminationThe proportion of zygotes that cleave to become embryos on Day 2 (44 ± 1 h post-insemination) .
Implantation rateUp to 30 days after transplantationThe number of gestational sacs divided by the total number of embryos transferred, irrespective of whether a pregnancy was established.
Clinical pregnancyUp to 30 days after transplantationA pregnancy diagnosed by ultrasonographic examination of at least one fetus with a discernible heartbeat.
MiscarriageUp to 42 weeks after transplantationThe spontaneous loss of an intrauterine pregnancy.
Live birthUp to 42 weeks after transplantationThe complete expulsion or extraction from a woman of a product of fertilization, after 20 completed weeks of gestational age.
Gestational age at birthUp to 42 weeks after transplantationThe age of a fetus is calculated by the best obstetric estimate determined by assessments which may include early ultrasound.
BirthweightUp to 42 weeks after transplantationBirth weight should be collected within 24 hours of birth and assessed using a calibrated electronic scale with ten-gram resolution.
Height of offspring 1 year oldUp to 1 year after deliverySelf-measurement

Secondary

MeasureTime frameDescription
Embryo development rateUp to 3 days after inseminationThe proportion of cleaved embryos at the 4-cell stage on Day 2 (44 ± 1 h post-insemination) or at the 8-cell stage on Day 3 (68 ± 1 h post-insemination) per normally fertilized oocyte.
1PN rateUp to 2 days after inseminationThe proportion of inseminated oocytes with one pronucleus on Day 1 (17 ± 1 h post-insemination).
Blastocyst development rateUp to 7 days after inseminationThe proportion of blastocysts observed at 116 ± 2 h post-insemination as a function of the number of normally fertilized oocytes.
Proportion of good blastocystsUp to 7 days after inseminationThe proportion of blastocysts with a grade of good or higher.
Ectopic pregnancyUp to 30 days after transplantationA pregnancy outside the uterine cavity, diagnosed by ultrasound, surgical visualization, or histopathology.
Gestational diabetesUp to 30 weeks after transplantationBy oral glucose tolerance test between 24 and 28 gestational weeks (fasting glucose ≥5.1 mmol/L, 1-h glucose ≥10.0 mmol/L, 2-h glucose ≥8.5 mmol/L; one abnormal result sufficient).
Gestational hypertensionUp to 42 weeks after transplantationMaternal systolic blood pressure ≥ 140 mmHg and (or) diastolic pressure ≥ 90 mmHg.
Major congenital anomalyUp to 42 weeks after transplantationStructural, functional, and genetic anomalies, that occur during pregnancy, and identified antenatally, at birth, or later in life, and require surgical repair of a defect, or are visually evident, or are life-threatening, or cause death.
Neonatal mortalityUp to 30 days after deliveryDeath of a live born baby within 28 days of birth.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 19, 2026