Condition: Shock · Shock, Septic · Hypotension · Sponsor: Odense University Hospital
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 and Swedish 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 and Swedish Emergency Departments.
This description comes directly from the study's public registry record.
Lasse P Bentsen, MD · +4520496950 · lasse.paludan.bentsen@rsyd.dk
Always discuss trial participation with your own doctor first.
| Bispebjerg Hospital | Copenhagen, Denmark | Recruiting |
| Esbjerg Hospital | Esbjerg, Denmark | Terminated |
| Gødstrup Regional Hospital | Herning, Denmark | Not Yet Recruiting |
| Zealand University Hospital | Køge, Denmark | Recruiting |
| Odense University Hospital | Odense, Denmark | Recruiting |
| Department of Emergency Medicine | Helsingborg, Sweden | Not Yet Recruiting |
| Department of Emergency Medicine | Linköping, Sweden | Not Yet Recruiting |
| Department of Emergency Medicine | Ystad, Sweden | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT05931601