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Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
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.
Peter
Horby
ergoresearch@ndm.ox.ac.uk
Corinne
Betts
pos-ari-er@ndm.ox.ac.uk
More information about this study, what is involved and how to take part can be found on the study website.
Acute upper respiratory infectionsOther acute lower respiratory infections
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.
POS-ARI-ER is an observational study recruiting adults attending hospital or acute healthcare settings with an acute respiratory infection. The study is designed to provide data for characterisation of respiratory infections and to serve as an infrastructure for rapid implementation of randomised controlled trials (RCTs)
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: Cohort study;
You can take part if:
You may not be able to take part if:
1)Patient has been transferred from another hospital 2)Patient admitted to hospital for > 2 days at the time of enrolment 3)Patient has been previously enrolled in the POS-ARI-ER study
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Corinne
Betts
pos-ari-er@ndm.ox.ac.uk
Peter
Horby
ergoresearch@ndm.ox.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 University Medical Centre Utrecht (Netherlands) and funded by European Commission .
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 54196
You can print or share the study information with your GP/healthcare provider or contact the research team directly.
