Live Stream of Prehospital point-of Care Ultrasound During Cardiopulmonary Resuscitation

Sponsor
Medical University of Vienna (Other)
Overall Status
Recruiting
CT.gov ID
NCT04817475
Collaborator
(none)
30
1
21
1.4

Study Details

Study Description

Brief Summary

Background: Point-of-care ultrasound (POCUS) has been suggested as a useful tool in out-of-hospital cardiac arrest (OHCA) for diagnosis and treatment of reversible causes. However, in prehospital emergency medicine performing ultrasound and the translation of the findings can be challenging. As new prehospital ultrasound devices offer the possibility for remote supervision, the impact of tele-supervision on the performance of POCUS during OHCA is unclear.

Aims: This prospective observational study aims to evaluate if POCUS with tele-supervision can be performed during CPR without any additional hands-off periods longer than 5 seconds.

Methods: In total 30 patients with OHCA, where POCUS is considered, will be included in this study.

Condition or Disease Intervention/Treatment Phase
  • Other: Point-of-care ultrasound with tele-supervision

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Live Stream of Prehospital point-of Care Ultrasound During Cardiopulmonary Resuscitation
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Mar 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Point-of-care ultrasound with tele-supervision

Point-of-care ultrasound of patients with a out-of-hospital cardiac arrest will be performed with tele-supervision.

Other: Point-of-care ultrasound with tele-supervision
Point-of-care ultrasound of patients with a out-of-hospital cardiac arrest will be performed with tele-supervision.

Outcome Measures

Primary Outcome Measures

  1. Hands-off time during prehospital cardiopulmonary resuscitation [through study completion, an average of 1 year]

    The primary outcome of this study evaluates, if POCUS with tele-supervision can be performed during prehospital cardiopulmonary resuscitation without any additional hands-off period longer than 5 seconds

Secondary Outcome Measures

  1. Impact of real-time supervision of POCUS during cardiopulmonary resuscitation on the duration time of POCUS [through study completion, an average of 1 year]

    Impact of real-time supervision of POCUS during cardiopulmonary resuscitation on the duration time of POCUS

  2. Impact of real-time supervision of POCUS during cardiopulmonary resuscitation on changing of diagnosis of suspected cause of out-of-hospital cardiac arrest. [through study completion, an average of 1 year]

    Impact of real-time supervision of POCUS during cardiopulmonary resuscitation on changing of diagnosis of suspected cause of out-of-hospital cardiac arrest.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patients with prehospital cardiac arrest, where POCUS is considered during cardiac pulmonary resuscitation, will be included.

Exclusion Criteria:
  • under the age of 18,

  • if POCUS is not considered or if POCUS will lead to a delay of live-saving treatment or transportation.

  • pregnant patients

  • patients with a body-mass-index (BMI) above 35 kg/m2

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of Vienna, Department of Anaesthesia & General Intensive Care Vienna Austria 1090

Sponsors and Collaborators

  • Medical University of Vienna

Investigators

  • Study Chair: Department of Anaesthesia & General Intensive Care, Medical University of Vienna

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Christina Hafner, Clinical Investigator, Medical University of Vienna
ClinicalTrials.gov Identifier:
NCT04817475
Other Study ID Numbers:
  • 2410/2020
First Posted:
Mar 26, 2021
Last Update Posted:
Jul 8, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Christina Hafner, Clinical Investigator, Medical University of Vienna

Study Results

No Results Posted as of Jul 8, 2022