Actively Recruiting
VAC-SIP-YF (Vaccination- Safety & Immunogenicity During Pregnancy- Yellow Fever)
Led by Institut Pasteur · Updated on 2025-12-15
270
Participants Needed
1
Research Sites
257 weeks
Total Duration
On this page
Sponsors
I
Institut Pasteur
Lead Sponsor
C
Cerballiance
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
VAC-SIP-YF (Vaccination- Safety & Immunogenicity During Pregnancy- Yellow Fever)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female gender
- Age over 18 years at the time of first yellow fever vaccination
- Oral consent obtained after being informed
- Covered by Social Security except Aide Médicale d'Etat
- For vaccination during pregnancy group: primary yellow fever vaccination given during pregnancy
- For vaccination outside pregnancy group: primary yellow fever vaccination given outside pregnancy
You will not qualify if you...
- Received a second yellow fever vaccination
- Unable to give informed consent
- Born in yellow fever endemic areas
- Under legal guardianship or trusteeship
- Medical condition preventing collection of 18.5 mL blood (for immunogenicity section)
- Did not give written consent for immunogenicity section participation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Medical Center of Institut Pasteur
Paris, France, 75015
Actively Recruiting
Research Team
K
Kaoutar JIDAR, MD
CONTACT
J
Julia ABAD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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