Sanofi Pasteur
Lyon, 69007, France
NCT Number: NCT05040802
The purpose of this study is to determine the effectiveness of Adacel against pertussis disease in infants < 2 months when administered during pregnancy following the current Advisory Committee on Immunization Practices (ACIP) recommendations, i.e., from 27 to 36 weeks of gestation, and 14 days or more before delivery.
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Notify Me2 day–2 month
All sexes
Observational
Lyon, 69007, France
The original study included cases recorded from 01 January 2011 through 31 December 2014, based on retrospective case-control methodology.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Cases were included if they met the following inclusion criteria:
Controls were included if they met the following inclusion criteria:
Exclusion criteria
Cases were excluded if they met any of the following exclusion criteria:
Controls were excluded if they met any of the following exclusion criteria:
Not applicable / dataset analysis
Time frame: During the data collection period (from 01 January 2011 to 31 December 2014)
Vaccine effectiveness at preventing pertussis in infants less than 2 months of age was estimated using conditional logistic regression.
Time frame: During the data collection period (from 01 January 2011 to 31 December 2014)
Vaccine effectiveness at preventing pertussis requiring hospitalization was estimated using conditional logistic regression
Sanofi Pasteur, a Sanofi Company
Industry
Effectiveness of Adacel Vaccination in Pregnancy at Preventing Pertussis in Infants < 2 Months of Age in the United States (US)
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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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