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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.
Stefan Ebmeyer, MD
00493302883
stefan.ebmeyer@thermofisher.com
Faranak Fassihianifard
00493302883
faranak.fassihianifard@thermofisher.com
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.
Emergency departments (ED) are becoming increasingly over-crowded, with patients facing prolonged waiting times. Therefore, a safe and rapid assessment that identifies patients with low severity that could be treated as outpatients is essential for improving the workflow within the ED.
The rationale of this IDEAL+ study is to safely decrease the number of hospital admissions through identification of low risk patients with the biomarker MR-proADM. This will has already been tested in the IDEAL - pilot study and results should be confirmed with this IDEAL+ study.
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:
You can take part if:
You may not be able to take part if:
This is in the inclusion criteria above
Below are the locations for where you can take part in the trial. Please note that not all sites may be open.
Faranak Fassihianifard
00493302883
faranak.fassihianifard@thermofisher.com
Stefan Ebmeyer, MD
00493302883
stefan.ebmeyer@thermofisher.com
The study is sponsored by Brahms AG
Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.
You can print or share the study information with your GP/healthcare provider or contact the research team directly.