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Safety of Tetanus, Diphtheria, Acellular Pertussis With 5 Acellular Pertussis Components (Tdap5) Vaccination During Pregnancy

Active, not recruiting
Conditions
Pertussis (Whooping Cough)
Interventions
Other: Not applicable / database analysis
Registration Number
NCT06258057
Lead Sponsor
Sanofi
Brief Summary

The purpose of this study is to evaluate the safety of Adacel vaccine among pregnant individuals exposed to Adacel at any point between the 1st day of the 27th week of gestation up to the end of pregnancy and their offspring (ie, Adacel-exposed cohort), in comparison with pregnant individuals not vaccinated with any Tdap vaccines during pregnancy and their offspring (ie, Tdap-unvaccinated comparator cohort).

The primary objectives are to estimate incidence rates and relative risks for each prespecified pregnancy outcome in Adacel-exposed and Tdap-unvaccinated comparator cohorts and for each prespecified adverse birth outcome in the offspring of both cohorts.

The secondary objectives are to estimate incidence rates and relative risks for each prespecified adverse fetal and neonatal outcome in the offspring of Adacel-exposed and Tdap unvaccinated comparator cohorts and for each prespecified adverse outcome for pregnant individuals in both cohorts.

Detailed Description

Study outcomes to be assessed in electronic medical records between January 2016 to December 2025.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
Female
Target Recruitment
365000
Inclusion Criteria
  • For pregnant individuals:

    • Continuous enrollment, with no more than a 1-month administrative gap from 90 days prior to their last menstrual period (LMP)
    • Continuous enrollment for the duration of their pregnancy through delivery or termination of pregnancy (or 6 weeks postpartum for preeclampsia/eclampsia and 28 days for PPH) unless censored at death in order to capture study outcomes
    • At least 1 prenatal visit prior to 27 weeks of gestation during pregnancy
  • For offspring:

    • Infants delivered by pregnant individuals who meet all the inclusion criteria above
    • With gestational age as calculated based on date of birth recorded in the EMR
Exclusion Criteria
  • For pregnant individuals:

    • Loss of pregnancy or with delivery before 27 weeks of gestation
    • Vaccinated with Boostrix® (Tdap vaccine, GSK), or with an unknown brand of Tdap vaccine, or Td (tetanus, diphtheria) vaccine during pregnancy
    • Vaccinated with any Tdap vaccine prior to the ACIP recommended optimal timeframe of ≥ 270/7 weeks of gestation
    • Received more than one Tdap vaccine during pregnancy
    • Vaccinated with one or more live vaccines during pregnancy
    • Pregnant individuals with multiple gestation pregnancies (eg, twins, triplets)
  • For offspring:

    • Infants delivered by pregnant individuals who meet any of the exclusion criteria above

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Tdap-Unvaccinated Comparator CohortNot applicable / database analysisCohort will include all pregnant individuals meeting eligibility criteria and with no record of any Tdap vaccination from pregnancy onset date until the end of pregnancy and their offspring
Adacel-Exposed CohortNot applicable / database analysisCohort will include all pregnant individuals with a record of Adacel vaccination during the third trimester of pregnancy (ie, first day of 27th week of gestation up to the end of pregnancy) and their offspring
Primary Outcome Measures
NameTimeMethod
Pregnancy outcome: Still birth/fetal demiseFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of still birth/fetal demise in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Birth outcome: Low birth weightFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of low birth weight in live born infants of both Adacel-exposed and Tdap-unvaccinated comparator cohorts

Birth outcome: Preterm birthFrom 1st day of the 27th week of gestation and less than 37 weeks gestation

Incidence rates of preterm birth in live born infants of both Adacel-exposed and Tdap-unvaccinated comparator cohorts

Birth outcome: Small for gestational ageFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of small for gestational age in live born infants of both Adacel-exposed and Tdap-unvaccinated comparator cohorts

Pregnancy outcome: Live birthFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of live births in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Pregnancy outcome: Therapeutic abortionFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of therapeutic abortion in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Secondary Outcome Measures
NameTimeMethod
Adverse neonatal outcome: Congenital anomaliesFrom birth up to 28 days post-birth

Incidence rates of congenital anomalies (major and minor) in the offspring of Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse fetal outcome: Fetal growth arrest (restriction)From 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of fetal growth arrest (restriction) in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: ChorioamnionitisFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of chorioamnionitis in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse neonatal outcome: Neonatal deathFrom birth up to 28 days post-birth

Incidence rates of neonatal death in the offspring of Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse neonatal outcome: Neonatal sepsisFrom birth up to 28 days post-birth

Incidence rates of neonatal sepsis in the offspring of Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: Preterm laborFrom 1st day of the 27th week of gestation and less than 37 weeks gestation

Incidence rates of Preterm labor in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: Preeclampsia/eclampsiaFrom 1st day of the 27th week of gestation up to 42 days postpartum

Incidence rates of preeclampsia/eclampsia in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: Postpartum hemorrhageWithin 24 hours of delivery up to 28 days postpartum

Incidence rates of postpartum hemorrhage in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: Placental abruptionFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of placental abruption in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse outcomes in pregnant individuals: Premature rupture of membranesFrom 1st day of the 27th week of gestation up to 42 weeks gestation

Incidence rates of premature rupture of membranes in Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse neonatal outcome: Neonatal respiratory distressFrom birth up to 28 days post-birth

Incidence rates of neonatal respiratory distress in the offspring of Adacel-exposed and Tdap-unvaccinated comparator cohorts

Adverse neonatal outcome: Neonatal/early infancy intensive care admissions for bronchopulmonary dysplasiaFrom birth up to 28 days post-birth

Incidence rates of neonatal/early infancy intensive care admissions for bronchopulmonary dysplasia in the offspring of Adacel-exposed and Tdap-unvaccinated comparator cohorts

Trial Locations

Locations (1)

Investigational Site

🇫🇷

Chilly-Mazarin, France

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