Image

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

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

Not Recruiting
15-49 years
Female
Phase N/A

Powered by AI

Overview

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.

Description

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

Eligibility

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 details
    Pertussis (Whooping Cough)

NCT06258057

Sanofi

12 December 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.