Live Stream of Prehospital Emergency Ultrasound in Patients With Acute Dyspnoea
NCT ID: NCT04817488
Last Updated: 2025-10-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
350 participants
OBSERVATIONAL
2021-07-01
2025-12-31
Brief Summary
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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).
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Prehospital emergency ultrasound with tele-supervision
Prehospital emergency ultrasound of patients with acute dyspnea will be performed with tele-supervision.
Prehospital emergency ultrasound with tele-supervision
Prehospital emergency ultrasound with tele-supervision in patients with acute dyspnoea
Prehospital emergency ultrasound without tele-supervision
Prehospital emergency ultrasound of patients with acute dyspnea will be performed without tele-supervision.
Prehospital emergency ultrasound without tele-supervision
Prehospital emergency ultrasound without tele-supervision in patients with acute dyspnoea
Interventions
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Prehospital emergency ultrasound with tele-supervision
Prehospital emergency ultrasound with tele-supervision in patients with acute dyspnoea
Prehospital emergency ultrasound without tele-supervision
Prehospital emergency ultrasound without tele-supervision in patients with acute dyspnoea
Eligibility Criteria
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Inclusion Criteria
* Respiratory rate \>20 breaths per minute
* Peripheral oxygen saturation without oxygen supplementation \<90%
Exclusion Criteria
* if PEU will lead to a delay of live-saving treatment or transportation
* if patient rejects the PEU, the patient will be excluded
18 Years
ALL
No
Sponsors
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Medical University of Vienna
OTHER
Responsible Party
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Christina Hafner
Clinical Investigator
Principal Investigators
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Department of Anaesthesia & General Intensive Care
Role: STUDY_CHAIR
Medical University of Vienna
Locations
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Medical University of Vienna, Department of Anaesthesia & General Intensive Care
Vienna, Vienna, Austria
Countries
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Other Identifiers
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2411/2020
Identifier Type: -
Identifier Source: org_study_id
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