Relevance of Reversible Causes During OHCA (Rebecca Study)
REBECCA
1 other identifier
interventional
100
1 country
2
Brief Summary
Management of the reversible causes in cardiac arrest is fundamental for successful treatment of out-of-hospital cardiac arrests. Point-of-care diagnostics as prehospital emergency ultrasound, blood gas analysis and toxicological screening support the diagnostic process of evaluating potential reversible causes. Digital tools provide support of a structured approach. This study aims to evaluate the frequency of reversible causes during OHCA as well as specific interventions due to these findings. Furthermore, CPR performance (hands-off, ROSC, 30-day mortality) and cognitive load of the prehospital emergency physician will be investigated. In total 100 patients with OHCA will be included in this study. Identification of reversible causes will be performed upon a structured protocol using an interactive checklist. Cognitive load of emergency physician as well as CPR parameter (frequency of reversible causes, hands-off, ROSC, 30-day mortality) will be analysed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Apr 2023
Longer than P75 for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 6, 2023
CompletedFirst Posted
Study publicly available on registry
March 27, 2023
CompletedStudy Start
First participant enrolled
April 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2026
ExpectedApril 20, 2026
April 1, 2026
2.8 years
January 6, 2023
April 15, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Frequency of reversible causes in OHCA and alterations of treatment
The primary outcome of this study evaluates the frequency of reversible causes during OHCA.
up to 30 days
Secondary Outcomes (4)
Frequency of ROSC
up to 30 days
30-day mortality
up to 30 days
Hands-off time
During study completion, up to 120 min
Cognitive load
1 year (evaluation in documentation phase after CPR)
Study Arms (1)
Evaluation of reversible causes using digital checklist and diagnostic support
OTHERInterventions
Prehospital evaluation by checklist and diagnostic testing for reversible causes of OHCA using point-of-care blood gas analysis, saliva toxicological screen and ultrasound and post-hoc toxicological analysis of blood using mass spectrometry
Eligibility Criteria
You may qualify if:
- Patients with prehospital cardiac arrest, where POCUS, blood gas analysis as well as screening for intoxication can integrated in ALS rhythm without delay of life-saving treatment or transportation will be included.
You may not qualify if:
- Patients will be excluded under the age of 18, or if POCUS, blood gas analysis will lead to a delay of live-saving treatment or transportation. Furthermore, pregnant patients will be excluded.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Seibersdorf Labor GmbHcollaborator
- Medical University of Viennalead
- Ludwig Boltzmann Institute for Digital Health and Preventioncollaborator
Study Sites (2)
Anesthesiology and Intensive Care Medicine Department - Medical University of Vienna
Vienna, 1090, Austria
Department of Anesthesia, General Intensive Care and Pain Management,Medical University of Vienna
Vienna, 1090, Austria
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
January 6, 2023
First Posted
March 27, 2023
Study Start
April 1, 2023
Primary Completion
December 31, 2025
Study Completion (Estimated)
December 31, 2026
Last Updated
April 20, 2026
Record last verified: 2026-04