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Clinical Trial Summary

Comparison of the sensibility and specificity of 3 different serological tests and evaluation of chicken pox immunity in pregnant women.

Secondary goals :

- Correlation memory / Immunity;

- Prevalence of VZV immunity in pregnant women;

- Evaluation of cellular and humoral immunity in cases with discrepancy between tests or between test and memory;

- Evaluation of acceptability of vaccination in the post partum period in non immune patients.

Methods Not randomized prospective study,

Number of patients : 400 Duration : 36 months Inclusion criteria : pregnant women >18years old, agree to participate (written consent) Exclusion criteria: auto immune disease, HIV +, grafted patients


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02775422
Study type Interventional
Source Hopital Foch
Contact
Status Terminated
Phase N/A
Start date March 30, 2015
Completion date July 26, 2020

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