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

Cincinnati Children's Hospital Medical Center logo

Cincinnati Children's Hospital Medical Center

Status

Enrolling

Conditions

Influenza

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT05436184
1U01AI144673-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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

Full description

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.

Enrollment

1,500 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

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

Trial design

1,500 participants in 1 patient group

Cincinnati IMPRINT birth cohort
Description:
mother-infant pairs enrolled at or after week 34 in pregnancy and followed over three flu seasons, up to four years of age.

Trial contacts and locations

1

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Central trial contact

Nancy Back, RN,MPH; Chelsea Rohlfs, MBA

Data sourced from clinicaltrials.gov

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