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Clinical Trials/NCT06426732
NCT06426732
Recruiting
Not Applicable

The Trajectory of Blood Pressure During Pregnancy in Assisted Reproductive Females

The Second Hospital of Shandong University1 site in 1 country2,000 target enrollmentNovember 1, 2022
ConditionsBlood Pressure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Blood Pressure
Sponsor
The Second Hospital of Shandong University
Enrollment
2000
Locations
1
Primary Endpoint
The Trajectory of Blood Pressure During Pregnancy in Assisted Reproductive Females
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The incidence of gestational hypertension and preeclampsia in the assisted reproductive technology population during pregnancy was significantly higher than that in the general normal pregnancy population. The use of assisted reproductive technology in this population due to infertility is often accompanied by many hypertension-related factors. We established a prospective cohort study based on assisted reproductive technology pregnancy population and natural pregnancy population. Through continuous monitoring of blood pressure changes and other risk factors during pregnancy in the two groups, we explored the trajectory trend and inflection point of assisted reproductive technology pregnancy population blood pressure during pregnancy. Through factor analysis, the risk factors of elevated blood pressure during pregnancy can be clearly identified, so as to carry out early intervention and strengthen the control of risk factors of elevated blood pressure in assisted reproductive technology population, in order to expect benign maternal and infant outcomes.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
June 30, 2025
Last Updated
last year
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Linlin Cui

Professor

The Second Hospital of Shandong University

Eligibility Criteria

Inclusion Criteria

  • Exposure group:
  • Mother: Seen in the obstetrics department of our hospital and meet the following conditions at the same time:
  • Complete at least one cycle of IVF or ICSI, PGD or IVM treatment (including natural cycles);
  • Clinical pregnancy was obtained after treatment. Offspring: Offspring born after in vitro fertilization-embryo transfer technique.
  • Non-exposed group:
  • Mother: A mother who conceived naturally. Offspring: 1) Offspring born by natural pregnancy. 2) Offspring born from natural pregnancy of exposed mothers.

Exclusion Criteria

  • Unwilling to participate in this research;
  • Unable to participate in this study due to special reasons, such as death, immigration, loss to follow-up;
  • Hereditary diseases, mental diseases, malignant tumors, pre-pregnancy hypertension, uterine malformations and other reproductive organ malformations;
  • Pregnant women who voluntarily terminate pregnancy due to non-preeclampsia factors;

Outcomes

Primary Outcomes

The Trajectory of Blood Pressure During Pregnancy in Assisted Reproductive Females

Time Frame: from pregnancy to delivery

The Trajectory of Blood Pressure During Pregnancy in Assisted Reproductive Females

Study Sites (1)

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