Personalised Risk assessment in Febrile illness to Optimise Real-life Management across the European Union (PERFORM) <br>
Completed
- Conditions
- febrile illness10019815
- Registration Number
- NL-OMON43233
- Lead Sponsor
- Radboud Universitair Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 1600
Inclusion Criteria
All children <18y presenting to the Emergency department or paediatric intensive care unit or other appropriate wards with fever, or a history of fever <72h, or a suspected infection, in whom the attending clinician determines the need for blood sampling. ;Healthy control children: • afebrile control children who are having blood tests for reasons other than for investigation of infectious or inflammatory illness.
Exclusion Criteria
Participation may not lead to an earlier need for blood transfusion.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method