Actively Recruiting

Age: 20Years - 49Years
FEMALE
ID05776082

Association of Cardiovascular Health During Pregnancy With Perinatal Outcomes - a Birth Cohort Study

Led by Women's Hospital School Of Medicine Zhejiang University · Updated on 2025-12-29

5000

Participants Needed

3

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pregnancy is a crucial time to assess and manage cardiovascular health risks for both mothers and their children. Researchers are studying the use of the American Heart Association's "Life's Essential 8" as a new way to evaluate cardiovascular health in pregnant women. The goal is to better understand how this tool can be applied and to develop appropriate cardiovascular health standards during pregnancy. The study involves observing pregnant women aged 20 to 49 who conceived naturally and are carrying a single baby. Participants will complete questionnaires, undergo clinical follow-ups, and provide specimens for analysis. The research focuses on monitoring cardiovascular health throughout pregnancy to explore its impact on pregnancy outcomes. During the study, researchers will track maternal and newborn health outcomes up to 42 weeks of gestation. Participants will be involved in routine prenatal checkups and data collection to support the study's assessments. This observational study helps gather important information on cardiovascular health during pregnancy without altering the standard care process.

CONDITIONS

Brief Title

Association of Gestational Cardiovascular Health With Pregnancy Outcomes

Who Can Participate

Age: 20Years - 49Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Maternal age between 20 and 49 years
  • Natural conception
  • Single pregnancy
  • Plan to have routine prenatal exams and deliver at the research center
Not Eligible

You will not qualify if you...

  • Diseases affecting metabolic function or life-threatening conditions before pregnancy
  • Assisted reproduction
  • Multiple pregnancy
  • Known fetal deformities or genetic defects
  • Incomplete clinical data

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 42 weeks until delivery completion

Participants undergo questionnaire surveys, clinical follow-up, and specimen collection during pregnancy to assess cardiovascular health and pregnancy outcomes.

Regular prenatal visits as per routine care schedule

Trial Site Locations

Total: 3 locations

1

Women's Hospital School Of Medicine Zhejiang University

Hangzhou, Zhejiang, China, 310006

Actively Recruiting

2

Taizhou First People's Hospital

Taizhou, Zhejiang, China, 310000

Actively Recruiting

3

Rwanda Society of Obstetricians and Gynecologists

Kigali, Rwanda

Active, Not Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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