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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Infections
  • Patients Presenting With Suspicion of Infection to the ED

NCT number NCT05108883
Study type Interventional
Source Brahms AG
Contact Faranak Fassihianifard
Phone 00493302883
Email faranak.fassihianifard@thermofisher.com
Status Recruiting
Phase N/A
Start date October 14, 2021
Completion date December 2023

See also
  Status Clinical Trial Phase
Completed NCT03770533 - Identifying Patients With Suspicion of Infection in the ED Who Have Low Disease Severity Using MR-proADM - Pilot Study N/A