Comparative Study of Tolerance and Immunogenicity Induced by Primary Yellow Fever Vaccination in Pregnant and Non-pregnant Women
Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
The aim of this study is to compare the immunogenicity induced by yellow fever vaccination administered during pregnancy with that induced by vaccination outside pregnancy, and to assess the maternal and fetal tolerance of this vaccination.
Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:
⁃ Common :
• Person over 18 years of age at the time of the first yellow fever vaccination
• Female gender
• Oral consent obtained after subject has been informed
• Subject covered by Social Security with the exception of Aide Médicale d'Etat
⁃ Specific to both groups :
• For women vaccinated during pregnancy (case): Primary yellow fever vaccination during pregnancy
• For women vaccinated outside pregnancy (control): Primary yellow fever vaccination outside pregnancy
Locations
Other Locations
France
Medical Center of Institut Pasteur
RECRUITING
Paris
Contact Information
Primary
Kaoutar JIDAR, MD
kaoutar.jidar@pasteur.fr
0140613817
Backup
Julia ABAD
julia.abad@pasteur.fr
Time Frame
Start Date: 2025-03-24
Estimated Completion Date: 2030-03
Participants
Target number of participants: 270
Treatments
Other: women vaccinated during pregnancy
Participants who received a yellow fever vaccination during pregnancy
Other: women vaccinated outside pregnancy
Participants who received a yellow fever vaccination outside pregnancy
Related Therapeutic Areas
Sponsors
Collaborators: Cerballiance
Leads: Institut Pasteur