Skip to content

The Effect of Periconceptional Phthalates Exposure on Couples' Reproductive Health

Periconceptional Phthalates Exposure and Its Epigenetic Effect on Fertility, Embryo Development, and Neonatal Outcomes: a Prospective Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03679000
Enrollment
2122
Registered
2018-09-20
Start date
2018-12-01
Completion date
2021-12-31
Last updated
2019-04-23

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

Conditions

Environmental Exposure, Infertility

Keywords

environmental exposure, epigenetic process, embryo development, infertility, cohort study

Brief summary

The study is a prospective cohort study, which is aiming to explore periconceptional phthalates exposure and its potential epigenetic effect on fertility, embryo development, and neonatal outcomes.

Detailed description

The study is a prospective cohort study, and its subjects are childbearing couples who are seeking assisted reproductive technologies for having a baby in the reproductive center in Tongji Hospital. 1. All enrolled couples will be needed to sign an informed consent and complete a questionnaire for collecting information about demographics, life-style, and medical and reproductive histories. 2. Biological samples will be collected from the participants to measure phthalates metabolites in order to evaluate the exposure of single person or the couple in different time phase.The samples include urine, blood that will be left after the hormones measurement for both spouses. The follicular fluid will be obtained from females on the day of oocyte retrieval. The left sperm samples after sperm analysis will be obtained from men. In the reproductive center of Tongji Hospital, hormone measurement for women and sperm analysis for men are required for the In vitro fertilization and embryo transfer in order to evaluate the fertility of couples.And the blastocyst culture medium will be obtained from couples after blastocyst transfer. All samples will be stored at -80℃ until further analysis. 3. Measurements of phthalates metabolites in the biological samples. 4. Collecting data from electronic medical records and follow-up.The basic information, clinical data and reproductive outcomes of the subjects will be collected by reviewing the electronic medical charts, including the height, weight, basic hormone levels, stimulation protocol and time, insemination protocol, fertilization rate, cleavage rate, excellent embryo rate, blastocyst formation rate, clinical pregnancy rate, as well as live birth rate,the newborns' height, weight, and gestational age, etc. 5. Analyze the miRNA expression profiles of blastocyst culture medium. 6. Statistical analysis. The investigators will analyze the association between the couples' phthalates exposure levels and the reproductive outcomes, and explore the association among periconceptional phthalates exposure, epigenetic changes and reproductive outcomes.

Interventions

None listed

Sponsors

Tongji Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

一. Inclusion and

Exclusion criteria

for primary study: The exclusion of men: 1. Occupational exposures 2. Couples living in separate places 3. Congenital diseases * Congenital azoospermia * Ejaculation dysfunction * Family history of genetic diseases 4. Acquired diseases * Genitourinary infections * Mumps * Endocrine diseases * Sexually transmitted diseases * Hyperthyroidism * Liver failure * Renal failure * Neurological diseases * Paraplegia * Acquired testicular injury 5. Patient who have received surgeries: * Inguinal hernia surgery * Vasectomy * Bladder neck surgery * Pelvic surgery 6. Patients who have used antitumor drugs and hormone The exclusion of women: 1. Occupational exposures 2. Couples living in separate places 3. Congenital gonadal dysplasia * Genital malformation * Chromosomal abnormalities * Family history of genetic diseases 4. Endocrine and metabolic diseases * Diabetes * Hyperprolactinemia * Thyroid and adrenal diseases 5. Cardiovascular diseases * Dyslipidemia * Systemic lupus erythematosus * Other rheumatic immune diseases 6. Patients who have received the following treatment: * Ovarian surgery * Thyroid surgery * Pituitary surgery * Anti-tumor radiotherapy * Chemotherapy 7. Patients with previous history as followed: * Endometrial injury * Endometrial polyps * Endometritis * Uterine fibroids * Endometriosis 8. Tubal effusion 二. Inclusive and exclusive criteria for blastocyst culture medium collection at the later stage. Inclusion criteria: 1. Subjects in the primary part of the study 2. ·Normal gender of men and women * No genetic diseases or congenital diseases * No family genetic history 3. Normal sperm analysis for men 4. Female age \<35 years 5. ·Normal Ovarian function for women * Normal endocrine function for women * No uterine disease or abnormality 6. The causes of infertility : * Tubal factors * Unexplained 7. The protocol of controlled ovary hyperstimulation : * A routine long-term protocol

Design outcomes

Primary

MeasureTime frameDescription
Phthalates exposure levels12/2021Concentrations of phthalates in ng/ml

Secondary

MeasureTime frameDescription
Exposure characteristics of phthalates12/2021The exposure of different personal care products in weeks
Reproductive outcomes12/2021The different reproductive outcomes in percent
The expression profiles of miRNA12/2021The expression profiles of miRNA in different quantity

Countries

China

Contacts

Primary ContactYufeng Li, Doctor
yufengli64@tjh.tjmu.edu.cn027-83663351

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026