The Effect of Periconceptional Phthalates Exposure on Couples' Reproductive Health

NCT ID: NCT03679000

Last Updated: 2019-04-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

2122 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-12-01

Study Completion Date

2021-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Environmental Exposure Infertility

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

The reproductive health of couples

The study is a prospective cohort study, and its participants are childbearing couples who are seeking assisted reproductive technologies for having a baby in the reproductive center in Tongji Hospital.The study is a observational study.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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

Exclusion Criteria

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.


1. Subjects with smoking or alcohol abuse in the past 3 months
2. Patients with overweight or obesity (BMI ≥ 25)
3. Embryos with chromosomal abnormalities confirmed by PGS
Minimum Eligible Age

20 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Tongji Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Liyufeng

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Yufeng Li, Doctor

Role: PRINCIPAL_INVESTIGATOR

Tongji Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Tongji Hospital

Wuhan, Hubei, China

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Yufeng Li, Doctor

Role: CONTACT

027-83663351

References

Explore related publications, articles, or registry entries linked to this study.

Du YY, Fang YL, Wang YX, Zeng Q, Guo N, Zhao H, Li YF. Follicular fluid and urinary concentrations of phthalate metabolites among infertile women and associations with in vitro fertilization parameters. Reprod Toxicol. 2016 Jun;61:142-50. doi: 10.1016/j.reprotox.2016.04.005. Epub 2016 Apr 8.

Reference Type BACKGROUND
PMID: 27067915 (View on PubMed)

Wang YX, Zeng Q, Sun Y, You L, Wang P, Li M, Yang P, Li J, Huang Z, Wang C, Li S, Dan Y, Li YF, Lu WQ. Phthalate exposure in association with serum hormone levels, sperm DNA damage and spermatozoa apoptosis: A cross-sectional study in China. Environ Res. 2016 Oct;150:557-565. doi: 10.1016/j.envres.2015.11.023. Epub 2015 Dec 3.

Reference Type BACKGROUND
PMID: 26654563 (View on PubMed)

Wang YX, You L, Zeng Q, Sun Y, Huang YH, Wang C, Wang P, Cao WC, Yang P, Li YF, Lu WQ. Phthalate exposure and human semen quality: Results from an infertility clinic in China. Environ Res. 2015 Oct;142:1-9. doi: 10.1016/j.envres.2015.06.010. Epub 2015 Jun 15.

Reference Type BACKGROUND
PMID: 26087406 (View on PubMed)

Zeng Q, Chen YZ, Xu L, Chen HX, Luo Y, Li M, Yue J, Liu AL, Li YF, Lu WQ. Evaluation of exposure to trihalomethanes in tap water and semen quality: a prospective study in Wuhan, China. Reprod Toxicol. 2014 Jul;46:56-63. doi: 10.1016/j.reprotox.2014.03.005. Epub 2014 Mar 13.

Reference Type BACKGROUND
PMID: 24632126 (View on PubMed)

Zeng Q, Li M, Xie SH, Gu LJ, Yue J, Cao WC, Zheng D, Liu AL, Li YF, Lu WQ. Baseline blood trihalomethanes, semen parameters and serum total testosterone: a cross-sectional study in China. Environ Int. 2013 Apr;54:134-40. doi: 10.1016/j.envint.2013.01.016. Epub 2013 Feb 26.

Reference Type BACKGROUND
PMID: 23454109 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

H0425

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Peking University Birth Cohort in Tongzhou
NCT03814395 ACTIVE_NOT_RECRUITING