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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.
Dr
Julie-Claire
Becher
julie-claire.becher@luht.scot.nhs.uk
Dr
Julie-Claire
Becher
julie-claire.becher@luht.scot.nhs.uk
This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.
This study will determine the incidence of sudden unexpected collpase in the early postnatal period of a previously well term infant. It will describe associated factors of such collapse an aims to establish safe guidelines for the optimal early postnatal care of all infantc. The association with infant position and feeding practices demands attention particularly as these are known risks in sudden infant death in older infants. We aim to demonstrate the widely disparate approach to investigation of these infants and highlight the need for a consensus in investigation.
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: Validation of investigation /therapeutic procedures;
You can take part if:
You may not be able to take part if:
Infants less than 37 weeks gestation; infants greater than 12 hours; infants who are not thought to be in a good cindition at birth.
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Dr
Julie-Claire
Becher
julie-claire.becher@luht.scot.nhs.uk
Dr
Julie-Claire
Becher
julie-claire.becher@luht.scot.nhs.uk
The study is sponsored by LOTHIAN and funded by WellChild .
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 10585
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
