Language: BG BG
← Back to results
Active (not recruiting) NCT04817488

Live Stream of Prehospital Emergency Ultrasound in Patients With Acute Dyspnoea

Conditions: Echocardiography Acute Dyspnea

Sponsor: Medical University of Vienna

trial.available_in: БГ
Overview
Background: Acute dyspnoea is a common symptom in prehospital emergency medicine. As ultrasound gained in importance for diagnosis in patients with acute respiratory distress, it plays even a role in the prehospital setting. However, prehospital emergency ultrasound (PEU) remains challenging and requires knowledge and skills. New prehospital ultrasound devices offer the possibility for tele-supervision. The impact of tele-supervision of PEU in patients with acute dyspnoea is unclear. Objective: This prospective observational study aims to evaluate the effect of PEU with tele-supervision on diagnosis, treatment strategies and cognitive load in comparison to PEU without tele-supervision in patients with acute dyspnoea. Methods: In total 350 prehospital emergency patients with acute dyspnoea will be included in this study. Patients will be observed in two groups. In group 1 PEU will be performed with tele-supervision, whereas in group 2 PEU will be performed without tele-supervision (tele-supervision not available).
Who can participate
Inclusion Criteria: Patients will be included, if they suffer from acute dyspnoea and at least one of the two following signs of respiratory failure: * Respiratory rate \>20 breaths per minute * Peripheral oxygen saturation without oxygen supplementation \<90% Exclusion Criteria: * under the age of 18 * if PEU will lead to a delay of live-saving treatment or transportation * if patient rejects the PEU, the patient will be excluded
Interventions
Prehospital emergency ultrasound with tele-supervision
OTHER
Prehospital emergency ultrasound without tele-supervision
OTHER
Locations 1
Austria (1)
Medical University of Vienna, Department of Anaesthesia & General Intensive Care
Vienna
Technical details
Status
Active (not recruiting)
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.07.2021
Completion date
31.12.2026
Registry ID
NCT04817488
Source
clinicaltrials.gov
trial.inquiry_btn

Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.