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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 provide guidance to safely decrease the number of hospital admissions through identification of low risk patients with the biomarker MR-proADM. This will be tested in a pilot study first.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03770533
Study type Interventional
Source Brahms AG
Contact
Status Completed
Phase N/A
Start date December 14, 2018
Completion date December 11, 2019

See also
  Status Clinical Trial Phase
Recruiting NCT05108883 - Risk Stratification Using Midregional Proadrenomedullin in the ED N/A