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Clinical Trials/NCT06180447
NCT06180447Active, not recruitingNot Applicable

Peri-conceptional or Pregnancy Exposure of Vaccination and the Risk of Adverse Pregnancy Outcomes

Sun Xin1 site in 1 country150,000 target enrollmentStarted: January 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
150,000
Locations
1
Primary Endpoint
Birth defects

Study Overview

Brief Summary

Uing data from a population based cohort in China, we will conduct retrospective cohort study to evaluate the risk of vaccine (e.g., HPV/influenza/rabies vaccine) administered during pregnancy (especially during first trimester) for adverse pregnancy outcomes (e.g., birth defects, preterm birth and low birth weight)

Detailed Description

We will develop a vaccination cohort by linking population-based pregnancy registries (i.e., REPRESENT) with population-based vaccine databases.

The researchers will use data from this cohort to examine vaccine use 90 days before the last menstrual period and throughout pregnancy. This study will investigate whether maternal vaccination during pregnancy is associated with the risk of adverse pregnancy outcomes. Poisson regression based on propensity scores will be used to estimate the relative risk. To ensure the robustness of the results, the researchers will perform several sensitivity analyses and negative control analyses, such as the risk of adverse pregnancy outcomes in pregnant women who have been vaccinated several times and pregnant women who have been vaccinated in mid and late pregnancy as negative control groups.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
14 Years to 65 Years (Child, Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • All pregnant women in Xiamen who registry in our database.

Exclusion Criteria

  • Pregnant women who were lost to follow-up. Pregnant women exposed to related factors of known congenital malformation.

Outcomes

Primary Outcomes

Birth defects

Time Frame: From pregnancy to 42 days after delivery

BDs were defined as any prenatal malformation (including structural, functional, or metabolic disorders) diagnosed through systematic ultrasound or genetic testing during pregnancy and any malformation diagnosed by clinicians within 42 days of birth,which were coded according to the International Classification of Diseases, Tenth Revision (ICD-10) (Q00-Q99).

Secondary Outcomes

  • Incidence of Adverse pregnancy outcomes(From pregnancy to 42 days after delivery)

Investigators

Sponsor
Sun Xin
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Sun Xin

professor; director

West China Hospital

Study Sites (1)

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