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Clinical Trial Summary

The goal of this pragmatic, multi-center, superiority, randomized clinical trial is to compare early treatment with peripheral (through a vein) infused noradrenaline (a natural hormone that increases blood pressure) with fluid only therapy in patients with hypotensive and shock in the Danish Emergency Departments (ED). The main questions it aims to answer are: If early initiated noradrenaline in non-bleeding hypotensive patients presenting in the ED can - Improve time to shock control. - Reduce the need for ICU admittance. - Decrease mortality. Participants will be included by the clinical staff and treated urgently with either noradrenaline or usual treatment during their Emergency Department stay. After completion of the treatment in the Emergency Department, patient data will be extracted from the bed-side measurements, electronic health records and national registers. Patients will be contacted by the research staff 1 year after study inclusion to answer brief questions about their daily physical function and ability to care for themselves. Researchers will compare with patients receiving fluid therapy only, as this is the usual standard of care in Danish Emergency Departments.


Clinical Trial Description

Please refer to the full protocol. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05931601
Study type Interventional
Source Odense University Hospital
Contact Lasse P Bentsen, MD
Phone +4520496950
Email lasse.paludan.bentsen@rsyd.dk
Status Recruiting
Phase Phase 3
Start date December 8, 2023
Completion date January 31, 2026

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