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OpenTrials
Active, Not Recruiting

NCT Number: NCT05436184

Influenza IMPRINT Cohort: Defining the Impact of Initial Influenza Exposure on Immunity in Infants

The primary aim is to define the immune responses to the infant's initial influenza exposure (vaccine or infection) and how that affects the immune response to subsequent influenza exposures

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45219, United States

About this study

Vaccination is a leading public health intervention for reducing morbidity and mortality from influenza worldwide. Vaccine optimization is hampered by lack of understanding the natural history of infection and immunity, including the full complement of maternal immunity imparted to infants. This gap in understanding can be addressed only through a well-designed birth cohort study. Up to 1500 mother-infant pairs will be enrolled at or after week 34 in pregnancy over three flu seasons, up to four years of age depending on birth month, at two sites. Follow-up will occur from the third trimester until the child is three to four years of age, along with medical records review to ascertain outcomes not captured through weekly illness and respiratory surveillance, and medical record review up to 18 years of age. The primary aim is to rigorously document the natural history of infection and immune response to influenza in study infants for at least three entire flu seasons.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Mother pregnant and ≥ 34 weeks gestation and ≥ 18 yrs. of age
  • Plans to deliver at local hospital
  • Lives within designated home zip codes:
  • No plans to move outside study area within study timeframe
  • Cell phone that can be used for text messaging
  • Singleton live born infant, born ≥ 34 weeks gestational age (GA)

Exclusion criteria

  • Fetal or infant death prior to maternal hospital discharge
  • Mother known to be infected with HIV based on medical records
  • Major congenital anomalies, prenatally diagnosed or other major disorder or anomaly as determined by the PI
  • Reported use of heroin, cocaine or methamphetamines during pregnancy
  • Adoptive infant
  • Enrolled in any investigational vaccine trial or other interventional randomized, clinical trial involving the mother or infant that the PI's deem to be in conflict with study outcomes

Treatment and study plan

Primary outcomes

  1. Immune response to influenza virus infection

    Time frame: 4 years

    Evaluate the immune response to influenza virus infections due to various subtypes in healthy children from birth to 4 years of age in a maternal-infant birth cohort

  2. Immune response to influenza vaccination

    Time frame: 4 years

    Evaluate the immune response to influenza vaccination in healthy children from 6 months to 4 years of age in a maternal-infant birth cohort

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Collaborators

  • National Institute of Allergy and Infectious Diseases (NIAID)

Registry information

Important dates

Study start
2019
Primary completion
2027
Study completion
2028
First posted
Jun 29, 2022
Registry last updated
Nov 5, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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