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Clinical Trial Summary

The purpose of this study is to determine the reasons why multiparous women (women who are pregnant and have been pregnant before) might still be susceptible to rubella.


Clinical Trial Description

This study is designed to investigate why multiparous women might still be susceptible to rubella. All pregnant women are checked for rubella immunity, and if they are non-immune, there are standard orders in our hospital to administer the rubella vaccine on the post-partum floor prior to discharge home from the hospital. Despite this, some multiparous women are found to be susceptible (non-immune), and this study will explore the reasons for this. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00401505
Study type Observational
Source St. Michael's Hospital, Toronto
Contact
Status Completed
Phase
Start date September 2006
Completion date September 2012

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