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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.
Natasha
Thorn
nthorn@sgul.ac.uk
Prof
Paul
Heath
pheath@sgul.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
Infections specific to the perinatal period
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Group B Streptococcus (GBS) is a bacterium (a bug) that causes serious infections in young infants across the world. In 2015 it was estimated that there were at least 319,000 infants under 3 months of age with GBS disease worldwide, resulting in 90,000 deaths and at least 10,000 children with long term disabilities. Around 20% of all pregnant women carry GBS in their vagina and bowel and babies are exposed to GBS bacteria around the time of birth. The options for prevention are currently limited to offering antibiotics during labour.
A vaccine that could be given to pregnant women has the greatest potential to benefit mothers and babies worldwide. There are vaccines currently being tested in clinical trials, including in pregnant women. The iGBS3 study aims to find out what levels of immunity (usually measured as antibody) a woman needs to pass to her baby to protect the baby from getting GBS disease. This will allow us to predict what antibody level a vaccine has to achieve to be effective and then to get those vaccines licensed and implemented as quickly as possible.
To do this, we need to take a small sample of cord blood from a very large number of women just after delivering their baby. We will need to follow around 180 000 babies in order to find at least 170 babies with GBS disease (of which 100 will have disease with the most common type) and compare their levels of antibody in cord blood with 300 healthy babies exposed to the same GBS type. To achieve this, we will work with the Nottingham Clinical Trials Unit to embed this study in their existing GBS3 Trial, in which 80 hospitals across England, Scotland and Wales will be involved for 2 years.
Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.
The recruitment start and end dates are as follows:
Observational type: Case-controlled study;
You can take part if:
You may not be able to take part if:
same as above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Natasha
Thorn
nthorn@sgul.ac.uk
Prof
Paul
Heath
pheath@sgul.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
The study is sponsored by St. George's Hospital Medical School and funded by Medical Research Council (MRC) .
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
Read full details
for Trial ID: CPMS 47256
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