Cardiac Arrest (CA)REVIVE ZugNCT07323667
A Study on the Impact of a New Canton-Wide First Responder System in Zug, Switzerland, on Survival After Adult Cardiac Arrest-Examining Early Life-Saving Organized Help, Fast Defibrillation, and Improved Outcomes for Out of Hospital Cardiac Arrest
An observational study of Cardiac Arrest (CA) and Cardiac Arrest With Successful Resuscitation, run by Felix Brinkmann at 1 site in Switzerland.
Trial summary
REVIVE Zug: Improving Emergency Response for Out-of-Hospital Cardiac Arrest Out-of-hospital cardiac arrest (OHCA) represents one of the most time-critical medical emergencies, where rapid recognition and immediate intervention are decisive for survival and neurological outcome. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Cardiac Arrest (CA), Cardiac Arrest With Successful Resuscitation, Resuscitation
- How many people
- 250 participants
- Where
- 1 siteSwitzerland
- Study dates
- 25 Jul 2025to 31 Aug 2027
- How long will I take part?
- 14 Days
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The study population will consist of individuals who experienced out-of-hospital cardiac arrest (OHCA) within the canton of Zug, Switzerland. Participants will be identified based on entries in local emergency medical services (EMS) registries and the national Swiss Reca registry. The population reflects all eligible OHCA cases attended by the Zug EMS, including both pre- and post-implementation periods of the First Responder system.
Who may be able to join
- Adults (18 years or older) who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug.
Who cannot join
- Patients younger than 18 years (pediatric cases).
- Patients with a documented refusal (written or verbal) to use data for research purposes.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Switzerland1 site
Rettungsdienst des Kantons Zug // Emergency Medical Service of the Canton Zug
Zug, Canton of Zug, 6300
About this study
Official title: REVIVE Zug: Impact of a Cantonal First Repsonder System on ROSC Rates and Incidence of Shockable Rhythms in Out-of-hospital Cardiac Arrest
REVIVE Zug: Improving Emergency Response for Out-of-Hospital Cardiac Arrest
Out-of-hospital cardiac arrest (OHCA) represents one of the most time-critical medical emergencies, where rapid recognition and immediate intervention are decisive for survival and neurological outcome. Early activation of emergency services, prompt initiation of cardiopulmonary resuscitation, and rapid defibrillation using automated external defibrillators (AEDs) are key components of the chain of survival. In many regions, organized First Responder systems-such as fire services, police forces, and trained lay responders supported by dispatcher-assisted instructions-arrive at the scene before emergency medical services (EMS) and initiate life-saving measures.
Read more
Evidence from multiple EMS systems indicates that the early involvement of First Responders is associated with higher rates of return of spontaneous circulation (ROSC) and improved survival to hospital discharge with favorable neurological outcomes. Regions with well-established First Responder networks consistently report better OHCA outcomes compared with regions without such systems.
In the canton of Zug, a comprehensive First Responder system has recently been implemented alongside an established hybrid EMS response model. In this system, resuscitation efforts are led either by an Emergency Physician (EP) or by a highly trained Critical Care Paramedic (CCP), depending on operational availability. Both roles operate within clearly defined competencies and provide the full scope of advanced prehospital care. This hybrid leadership model offers a unique opportunity to examine whether the professional background of the team leader influences resuscitation outcomes in real-world clinical practice.
The REVIVE Zug study aims to evaluate the impact of the canton-wide First Responder system on outcomes following OHCA. Key outcomes of interest include ROSC rates, hospital admission after cardiac arrest, the occurrence of shockable rhythms at EMS arrival, and outcomes achieved before EMS arrival. In addition, the study explores whether team leadership by an EP or a CCP is associated with differences in resuscitation outcomes. Further analyses focus on time intervals within the chain of survival, such as time from cardiac arrest to arrival of organized help and time to first defibrillation, as well as on event timing and basic demographic characteristics.
The study is based on anonymized data from established EMS quality registries and the national Swiss Reca database. By comparing OHCA cases before and after implementation of the comprehensive First Responder system, the project seeks to provide robust, practice-oriented evidence to inform future development of prehospital emergency care systems in Switzerland and comparable settings.
Read the detailed description
Background and Rationale
Out-of-hospital cardiac arrest (OHCA) remains one of the leading causes of prehospital mortality and represents a medical emergency with extreme time sensitivity. Survival and neurological outcome are strongly dependent on early recognition, rapid activation of the emergency response system, immediate high-quality cardiopulmonary resuscitation, and timely defibrillation. Delays at any stage of the chain of survival substantially reduce the likelihood of return of spontaneous circulation (ROSC) and survival to hospital discharge.
Organized First Responder systems, including fire services, police units, and trained lay responders supported by dispatcher-assisted cardiopulmonary resuscitation, have been shown to strengthen the early phases of OHCA management. These responders frequently arrive before emergency medical services (EMS) and initiate life-saving interventions during the critical first minutes after collapse. Regions with structured First Responder programs consistently report higher ROSC rates, shorter time to first defibrillation, and improved survival compared with regions without such systems.
In the canton of Zug, Switzerland, EMS operates within a hybrid response model in which resuscitation teams are led either by an Emergency Physician (EP) or by a highly trained Critical Care Paramedic (CCP), depending on operational availability. CCPs have completed advanced postgraduate training and operate with a high degree of autonomy within clearly defined delegated competencies. Both EPs and CCPs are authorized to provide the full range of advanced prehospital resuscitation care. This model reflects a pragmatic approach to maintaining high-quality emergency coverage while allowing flexibility in staffing.
The coexistence of a canton-wide First Responder system and a hybrid EMS leadership model provides a unique opportunity to evaluate system-level effects on OHCA outcomes within a real-world Swiss setting. While international literature suggests that overall survival outcomes are broadly comparable between physician-led and paramedic-led resuscitations, ongoing debate persists regarding potential differences in specific subgroups or early resuscitation endpoints. At the same time, evidence increasingly emphasizes that early intervention by First Responders may have a greater population-level impact than the professional background of the advanced life support team leader.
Despite the widespread implementation of First Responder programs in Switzerland, systematic evaluation in the German-speaking regions remains limited. REVIVE Zug addresses this gap by providing a comprehensive analysis of OHCA outcomes before and after implementation of a full-coverage First Responder system, while accounting for the potential influence of EMS team leadership.
Objectives
The primary objective of the REVIVE Zug study is to assess the impact of a canton-wide First Responder system on outcomes following out-of-hospital cardiac arrest.
Primary outcomes include:
Rates of return of spontaneous circulation
Rates of hospital admission following OHCA
Occurrence of shockable cardiac rhythms at EMS arrival
Achievement of ROSC prior to arrival of EMS
Secondary objectives focus on evaluating whether the type of EMS team leadership-Emergency Physician versus Critical Care Paramedic-is associated with differences in resuscitation outcomes once EMS-led care has begun. Additional analyses examine key time intervals within the chain of survival, including time from cardiac arrest to arrival of organized help and time to first defibrillation. Event timing characteristics (such as time of day and weekday versus weekend occurrence) and basic demographic factors are also assessed to support contextual interpretation of results.
Study Design
REVIVE Zug is an ambispective observational data analysis combining retrospective and prospective cohorts. The retrospective cohort includes OHCA cases occurring prior to implementation of the comprehensive First Responder system, while the prospective cohort includes cases managed after full system deployment.
The study uses encrypted, non-genetic, health-related personal data derived from established registries, including the local EMS quality registry and the national Swiss Reca resuscitation registry. Data collection follows standardized documentation procedures using routine EMS records and case report forms. For prospective data, an additional structured case report form for First Responder interventions has been introduced to address potential documentation gaps.
Only adult OHCA cases occurring within the canton of Zug are included. Pediatric cases are excluded due to low case numbers. Cases with a documented refusal for data use are excluded.
Data Management and Statistical Approach
All data are pseudonymized at the point of entry and fully anonymized for analysis. Linkage keys are stored separately and accessible only to a limited number of specifically authorized individuals. Data are stored on encrypted, password-protected servers within the Health Directorate of the canton of Zug.
Statistical analyses are exploratory and descriptive in nature. Continuous variables are summarized using mean and standard deviation or median and range, depending on data distribution. Categorical and ordinal variables are reported as counts and proportions. Group comparisons are conducted using appropriate statistical tests based on data characteristics, including parametric and non-parametric methods. Correlation analyses are performed using established statistical coefficients as appropriate. Standard statistical software packages are used for analysis and graphical presentation.
Based on historical data, the expected annual number of OHCA cases in the study region is approximately 40 cases per year, resulting in an estimated total sample size of around 250 cases across the full study period.
Data Sources and Security
Study data originate from the Swiss Reca registry and the internal EMS quality registry, both of which have long-standing experience with standardized, pseudonymized data collection. EMS mission reports and routine documentation are archived in accordance with cantonal quality assurance procedures.
All study data are centrally stored within the Health Directorate of Zug. Access is strictly limited to authorized personnel through role-based permissions. Audit trails, access logging, and data integrity controls are in place. Data handling follows established clean-desk and information security policies.
Ethical Considerations and Regulatory Compliance
Due to the acute nature of OHCA and the high associated mortality, it is often not feasible to obtain individual informed consent retrospectively. The study therefore operates under an exemption in accordance with Article 34 of the Swiss Human Research Act for the use of anonymized health-related data. This exemption has been granted by the responsible ethics committee for Northwest and Central Switzerland.
No data are included if a written or verbal refusal has been documented. All individuals with access to coded or operational data are subject to Swiss medical confidentiality obligations and official secrecy requirements. Patient data are retained for a minimum of five years in accordance with Swiss quality assurance and regulatory standards.
The study complies with the Swiss Human Research Act and Human Research Ordinance. Any protocol amendments or changes in project responsibility are documented and reported in accordance with regulatory requirements.
Anticipated Outcomes and Relevance
REVIVE Zug aims to provide a differentiated, practice-oriented assessment of how a comprehensive First Responder system influences OHCA outcomes within a real-world EMS environment. By integrating operational data with standardized registry information, the study seeks to generate findings that are relevant to EMS system design, responder training, and emergency planning.
The results are expected to support evidence-based decisions regarding early response strategies and the organization of prehospital care. Findings will be disseminated through scientific publication and professional exchange, with the goal of informing future improvements in OHCA management in Switzerland and comparable healthcare systems.
- Conditions
- Cardiac Arrest (CA), Cardiac Arrest With Successful Resuscitation, Resuscitation, Emergency Medical Services, First Aid, Defibrillators
- Keywords
- OHCA, Resuscitation, First responder, AED, Automated external Defibrillator, Return of spontaneous circulation, ROSC, Critical care paramedic, Emergency physician, Prehsopital care, Paramedic-led care, Physician-led care, Switzerland
- Medical subject headings
- Heart Arrest
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Cohort 1: Patients with OHCA before the implementation of First Responder system (retropersp.) | Cohort 1: Pre-Implementation Group Patients who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug before the introduction of the comprehensive First Responder system (retrospective cohort). | |
| Cohort 1: Patients with OHCA after the implementation of First Responder system (propersp.) | Cohort 2: Post-Implementation Group Patients who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug after the introduction of the comprehensive First Responder system (prospective cohort). |
What is being measured
The primary outcome is the main question the study is designed to answer.
Return of Spontaneous Circulation (ROSC) prior to arrival of EMS.
Definition: Number and proportion of out-of-hospital cardiac arrest (OHCA) patients achieving ROSC prior to arrival of EMS.
Measured: Time Frame: From cardiac arrest onset (as recorded by bystander/witness or dispatch log) until EMS arrival on scene (time-stamped in EMS run sheet); assessed up to 60 minutes.
Hospital admission after OHCA
Definition: Number and proportion of OHCA patients who are admitted to the hospital (survived to hand-over at the emergency department or ICU).
Measured: From cardiac arrest onset until documented handover at the ED or ICU (time-stamped in EMS/hospital record); assessed up to 24 hours.
Occurrence of shockable rhythm at EMS arrival
Definition: Number and proportion of patients presenting with a shockable cardiac rhythm (ventricular fibrillation/pulseless ventricular tachycardia) upon first EMS assessment.
Measured: Baseline (initial rhythm documented at EMS arrival on scene).
Secondary outcomes (7)
Prehospital resuscitation outcome by EMS team leadership (Emergency Physician vs Critical Care Paramedic)
Number and proportion of out-of-hospital cardiac arrest (OHCA) patients with the following prehospital resuscitation outcomes, analyzed by EMS team leadership type:
ROSC at hospital handover: sustained return of spontaneous circulation with transport and handover at the emergency department (ED) or ICU while in ROSC, or Death pronounced on scene: termination of resuscitation with death pronounced on scene.
Leadership category determined by EMS team leader profession (Emergency Physician [EP] or Critical Care Paramedic [CCP]) at the incident.
Measured: From EMS arrival on scene until hospital handover (ED/ICU) while in ROSC or death pronounced on scene; assessed up to 6 hours.
Time from Cardiac Arrest to Arrival of Organized Help
Definition: Measured interval (minutes) from estimated time of OHCA to arrival of the first organized responder (EMS or First Responder).
Measured: Baseline (index OHCA event; prehospital interval, measured once).
Time to First Defibrillation
Definition: Interval (minutes) from time of cardiac arrest to delivery of first defibrillation.
Measured: From estimated cardiac arrest onset (witness/dispatch record) until first defibrillation (defibrillator time-stamp/EMS record); assessed up to 60 minutes.
Event Timing
Distribution of out-of-hospital cardiac arrest events by time of day (day vs. night).
Measured: At cardiac arrest onset (baseline).
Demographics (Age, Gender)
Descriptive analysis of patient demographics, including age and sex.
Measured: Baseline (at cardiac arrest onset)
Day of week of cardiac arrest occurrence
Distribution of out-of-hospital cardiac arrest events by weekday versus weekend.
Measured: At cardiac arrest onset (baseline)
Date and calendar distribution of cardiac arrest events
Distribution of out-of-hospital cardiac arrest events by calendar date.
Measured: At cardiac arrest onset (baseline)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted7 Jan 2026
- Study start25 Jul 2025
- Primary completion30 Jun 2027 (estimated)
- Study completion31 Aug 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (10)Papers the sponsor has linked to this study.
- Other trials for Cardiac Arrest (CA)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Other
- Enrolment
- 250 participants (estimated)
- Target duration
- 14 Days
Sponsor and investigators
- Lead sponsor
- Felix Brinkmann
- Sponsor type
- Other government
- Responsible party
- Sponsor-investigator, Felix Brinkmann, Rettungsdienst Zug
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07323667
- Sponsor's protocol ID
- 2025-01169
- Other IDs
- 2025
- Acronym
- REVIVE Zug
- Status last verified
- Jun 2025
- First submitted
- 25 Jun 2025
- Last updated
- 7 Jan 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: At this time, we do not plan to share individual participant data (IPD) outside the study team due to data protection requirements and restrictions in the consent and ethics approval. Data may be available upon reasonable request to the corresponding author and subject to additional ethical approval. Ethic committee permission and strict Swiss data protection guidelines apply.
Publications
Bjornsson HM, Bjornsdottir GG, Olafsdottir H, Mogensen BA, Mogensen B, Thorgeirsson G. Effect of replacing ambulance physicians with paramedics on outcome of resuscitation for prehospital cardiac arrest. Eur J Emerg Med. 2021 Jun 1;28(3):227-232. doi: 10.1097/MEJ.0000000000000786.
PubMed 33709992Bujak K, Nadolny K, Trzeciak P, Galazkowski R, Ladny JR, Gasior M. Does the presence of physician-staffed emergency medical services improve the prognosis in out-of-hospital cardiac arrest? A propensity score matching analysis. Kardiol Pol. 2022;80(6):685-692. doi: 10.33963/KP.a2022.0109. Epub 2022 Apr 21.
PubMed 35445741Kern M, Jansen G, Strickmann B, Kerner T. Advancements in Public First Responder Programs for Out-of-Hospital Cardiac Arrest: An Updated Literature Review. Rev Cardiovasc Med. 2025 Jan 22;26(1):26140. doi: 10.31083/RCM26140. eCollection 2025 Jan.
PubMed 39867188Schwaiger D, Krosbacher A, Eckhardt C, Schausberger L, Baubin M, Rajsic S. Out-of-hospital cardiac arrest: A 10-year analysis of survival and neurological outcomes. Heart Lung. 2025 Sep-Oct;73:1-8. doi: 10.1016/j.hrtlng.2025.04.003. Epub 2025 Apr 18.
PubMed 40250261Oosterveer DM, de Visser M, Heringhaus C. Improved ROSC rates in out-of-hospital cardiac arrest patients after introduction of a text message alert system for trained volunteers. Neth Heart J. 2023 Jan;31(1):36-41. doi: 10.1007/s12471-021-01656-6. Epub 2022 Jan 6.
PubMed 34993887Oving I, de Graaf C, Masterson S, Koster RW, Zwinderman AH, Stieglis R, AliHodzic H, Baldi E, Betz S, Cimpoesu D, Folke F, Rupp D, Semeraro F, Truhlar A, Tan HL, Blom MT; ESCAPE-NET Investigators. European first responder systems and differences in return of spontaneous circulation and survival after out-of-hospital cardiac arrest: A study of registry cohorts. Lancet Reg Health Eur. 2020 Nov 20;1:100004. doi: 10.1016/j.lanepe.2020.100004. eCollection 2021 Feb.
PubMed 35104306Nehme Z, Andrew E, Bernard S, Haskins B, Smith K. Trends in survival from out-of-hospital cardiac arrests defibrillated by paramedics, first responders and bystanders. Resuscitation. 2019 Oct;143:85-91. doi: 10.1016/j.resuscitation.2019.08.018. Epub 2019 Aug 17.
PubMed 31430512Krammel M, Lobmeyr E, Sulzgruber P, Winnisch M, Weidenauer D, Poppe M, Datler P, Zeiner S, Keferboeck M, Eichelter J, Hamp T, Uray T, Schnaubelt S, Nuernberger A. The impact of a high-quality basic life support police-based first responder system on outcome after out-of-hospital cardiac arrest. PLoS One. 2020 Jun 2;15(6):e0233966. doi: 10.1371/journal.pone.0233966. eCollection 2020.
PubMed 32484818Siman-Tov M, Strugo R, Podolsky T, Rosenblat I, Blushtein O. Impact of dispatcher assisted CPR on ROSC rates: A National Cohort Study. Am J Emerg Med. 2021 Jun;44:333-338. doi: 10.1016/j.ajem.2020.04.037. Epub 2020 Apr 15.
PubMed 32336582Salhi RA, Hammond S, Lehrich JL, O'leary M, Kamdar N, Brent C, Mendes de Leon CF, Mendel P, Nelson C, Forbush B, Neumar R, Nallamothu BK, Abir M; CARES Surveillance Group. The association of fire or police first responder initiated interventions with out of hospital cardiac arrest survival. Resuscitation. 2022 May;174:9-15. doi: 10.1016/j.resuscitation.2022.02.026. Epub 2022 Mar 4.
PubMed 35257834
Study at a glance
From the registry record, last updated by the sponsor on 7 Jan 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- REVIVE Zug: Impact of a Cantonal First Repsonder System on ROSC Rates and Incidence of Shockable Rhythms in Out-of-hospital Cardiac Arrest
- ClinicalTrials.gov ID
- NCT07323667
- Acronym / sponsor ID
- REVIVE Zug / 2025-01169
- Conditions
- Cardiac Arrest (CA), Cardiac Arrest With Successful Resuscitation, Resuscitation, Emergency Medical Services, First Aid, Defibrillators
- Keywords
- OHCA, Resuscitation, First responder, AED, Automated external Defibrillator, Return of spontaneous circulation, ROSC, Critical care paramedic
- Study type
- Observational
- Recruitment status
- Enrolling by invitation
- Enrolment
- 250 participants (estimated)
- Lead sponsor
- Felix BrinkmannOther government
- Study start
- 25 Jul 2025 (actual)
- Primary completion
- 30 Jun 2027 (estimated)
- Study completion
- 31 Aug 2027 (estimated)
- First posted
- 7 Jan 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
REVIVE Zug: Improving Emergency Response for Out-of-Hospital Cardiac Arrest
Out-of-hospital cardiac arrest (OHCA) represents one of the most time-critical medical emergencies, where rapid recognition and immediate intervention are decisive for survival and neurological outcome. Early activation of emergency services, prompt initiation of cardiopulmonary resuscitation, and rapid defibrillation using automated external defibrillators (AEDs) are key components of the chain of survival. In many regions, organized First Responder systems-such as fire services, police forces, and trained lay responders supported by dispatcher-assisted instructions-arrive at the scene before emergency medical services (EMS) and initiate life-saving measures.
Evidence from multiple EMS systems indicates that the early involvement of First Responders is associated with higher rates of return of spontaneous circulation (ROSC) and improved survival to hospital discharge with favorable neurological outcomes. Regions with well-established First Responder networks consistently report better OHCA outcomes compared with regions without such systems.
In the canton of Zug, a comprehensive First Responder system has recently been implemented alongside an established hybrid EMS response model. In this system, resuscitation efforts are led either by an Emergency Physician (EP) or by a highly trained Critical Care Paramedic (CCP), depending on operational availability. Both roles operate within clearly defined competencies and provide the full scope of advanced prehospital care. This hybrid leadership model offers a unique opportunity to examine whether the professional background of the team leader influences resuscitation outcomes in real-world clinical practice.
The REVIVE Zug study aims to evaluate the impact of the canton-wide First Responder system on outcomes following OHCA. Key outcomes of interest include ROSC rates, hospital admission after cardiac arrest, the occurrence of shockable rhythms at EMS arrival, and outcomes achieved before EMS arrival. In addition, the study explores whether team leadership by an EP or a CCP is associated with differences in resuscitation outcomes. Further analyses focus on time intervals within the chain of survival, such as time from cardiac arrest to arrival of organized help and time to first defibrillation, as well as on event timing and basic demographic characteristics.
The study is based on anonymized data from established EMS quality registries and the national Swiss Reca database. By comparing OHCA cases before and after implementation of the comprehensive First Responder system, the project seeks to provide robust, practice-oriented evidence to inform future development of prehospital emergency care systems in Switzerland and comparable settings.
Detailed description
Background and Rationale
Out-of-hospital cardiac arrest (OHCA) remains one of the leading causes of prehospital mortality and represents a medical emergency with extreme time sensitivity. Survival and neurological outcome are strongly dependent on early recognition, rapid activation of the emergency response system, immediate high-quality cardiopulmonary resuscitation, and timely defibrillation. Delays at any stage of the chain of survival substantially reduce the likelihood of return of spontaneous circulation (ROSC) and survival to hospital discharge.
Organized First Responder systems, including fire services, police units, and trained lay responders supported by dispatcher-assisted cardiopulmonary resuscitation, have been shown to strengthen the early phases of OHCA management. These responders frequently arrive before emergency medical services (EMS) and initiate life-saving interventions during the critical first minutes after collapse. Regions with structured First Responder programs consistently report higher ROSC rates, shorter time to first defibrillation, and improved survival compared with regions without such systems.
In the canton of Zug, Switzerland, EMS operates within a hybrid response model in which resuscitation teams are led either by an Emergency Physician (EP) or by a highly trained Critical Care Paramedic (CCP), depending on operational availability. CCPs have completed advanced postgraduate training and operate with a high degree of autonomy within clearly defined delegated competencies. Both EPs and CCPs are authorized to provide the full range of advanced prehospital resuscitation care. This model reflects a pragmatic approach to maintaining high-quality emergency coverage while allowing flexibility in staffing.
The coexistence of a canton-wide First Responder system and a hybrid EMS leadership model provides a unique opportunity to evaluate system-level effects on OHCA outcomes within a real-world Swiss setting. While international literature suggests that overall survival outcomes are broadly comparable between physician-led and paramedic-led resuscitations, ongoing debate persists regarding potential differences in specific subgroups or early resuscitation endpoints. At the same time, evidence increasingly emphasizes that early intervention by First Responders may have a greater population-level impact than the professional background of the advanced life support team leader.
Despite the widespread implementation of First Responder programs in Switzerland, systematic evaluation in the German-speaking regions remains limited. REVIVE Zug addresses this gap by providing a comprehensive analysis of OHCA outcomes before and after implementation of a full-coverage First Responder system, while accounting for the potential influence of EMS team leadership.
Objectives
The primary objective of the REVIVE Zug study is to assess the impact of a canton-wide First Responder system on outcomes following out-of-hospital cardiac arrest.
Primary outcomes include:
Rates of return of spontaneous circulation
Rates of hospital admission following OHCA
Occurrence of shockable cardiac rhythms at EMS arrival
Achievement of ROSC prior to arrival of EMS
Secondary objectives focus on evaluating whether the type of EMS team leadership-Emergency Physician versus Critical Care Paramedic-is associated with differences in resuscitation outcomes once EMS-led care has begun. Additional analyses examine key time intervals within the chain of survival, including time from cardiac arrest to arrival of organized help and time to first defibrillation. Event timing characteristics (such as time of day and weekday versus weekend occurrence) and basic demographic factors are also assessed to support contextual interpretation of results.
Study Design
REVIVE Zug is an ambispective observational data analysis combining retrospective and prospective cohorts. The retrospective cohort includes OHCA cases occurring prior to implementation of the comprehensive First Responder system, while the prospective cohort includes cases managed after full system deployment.
The study uses encrypted, non-genetic, health-related personal data derived from established registries, including the local EMS quality registry and the national Swiss Reca resuscitation registry. Data collection follows standardized documentation procedures using routine EMS records and case report forms. For prospective data, an additional structured case report form for First Responder interventions has been introduced to address potential documentation gaps.
Only adult OHCA cases occurring within the canton of Zug are included. Pediatric cases are excluded due to low case numbers. Cases with a documented refusal for data use are excluded.
Data Management and Statistical Approach
All data are pseudonymized at the point of entry and fully anonymized for analysis. Linkage keys are stored separately and accessible only to a limited number of specifically authorized individuals. Data are stored on encrypted, password-protected servers within the Health Directorate of the canton of Zug.
Statistical analyses are exploratory and descriptive in nature. Continuous variables are summarized using mean and standard deviation or median and range, depending on data distribution. Categorical and ordinal variables are reported as counts and proportions. Group comparisons are conducted using appropriate statistical tests based on data characteristics, including parametric and non-parametric methods. Correlation analyses are performed using established statistical coefficients as appropriate. Standard statistical software packages are used for analysis and graphical presentation.
Based on historical data, the expected annual number of OHCA cases in the study region is approximately 40 cases per year, resulting in an estimated total sample size of around 250 cases across the full study period.
Data Sources and Security
Study data originate from the Swiss Reca registry and the internal EMS quality registry, both of which have long-standing experience with standardized, pseudonymized data collection. EMS mission reports and routine documentation are archived in accordance with cantonal quality assurance procedures.
All study data are centrally stored within the Health Directorate of Zug. Access is strictly limited to authorized personnel through role-based permissions. Audit trails, access logging, and data integrity controls are in place. Data handling follows established clean-desk and information security policies.
Ethical Considerations and Regulatory Compliance
Due to the acute nature of OHCA and the high associated mortality, it is often not feasible to obtain individual informed consent retrospectively. The study therefore operates under an exemption in accordance with Article 34 of the Swiss Human Research Act for the use of anonymized health-related data. This exemption has been granted by the responsible ethics committee for Northwest and Central Switzerland.
No data are included if a written or verbal refusal has been documented. All individuals with access to coded or operational data are subject to Swiss medical confidentiality obligations and official secrecy requirements. Patient data are retained for a minimum of five years in accordance with Swiss quality assurance and regulatory standards.
The study complies with the Swiss Human Research Act and Human Research Ordinance. Any protocol amendments or changes in project responsibility are documented and reported in accordance with regulatory requirements.
Anticipated Outcomes and Relevance
REVIVE Zug aims to provide a differentiated, practice-oriented assessment of how a comprehensive First Responder system influences OHCA outcomes within a real-world EMS environment. By integrating operational data with standardized registry information, the study seeks to generate findings that are relevant to EMS system design, responder training, and emergency planning.
The results are expected to support evidence-based decisions regarding early response strategies and the organization of prehospital care. Findings will be disseminated through scientific publication and professional exchange, with the goal of informing future improvements in OHCA management in Switzerland and comparable healthcare systems.
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Target follow-up
- 14 Days
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Cohort 1: Patients with OHCA before the implementation of First Responder system (retropersp.) | – | –Cohort 1: Pre-Implementation Group Patients who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug before the introduction of the comprehensive First Responder system (retrospective cohort). |
| Cohort 1: Patients with OHCA after the implementation of First Responder system (propersp.) | – | –Cohort 2: Post-Implementation Group Patients who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug after the introduction of the comprehensive First Responder system (prospective cohort). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The study population will consist of individuals who experienced out-of-hospital cardiac arrest (OHCA) within the canton of Zug, Switzerland. Participants will be identified based on entries in local emergency medical services (EMS) registries and the national Swiss Reca registry. The population reflects all eligible OHCA cases attended by the Zug EMS, including both pre- and post-implementation periods of the First Responder system.
Key inclusion criteria (1 listed)
- Adults (18 years or older) who experienced out-of-hospital cardiac arrest (OHCA) in the canton of Zug.
Key exclusion criteria (2 listed)
- Patients younger than 18 years (pediatric cases).
- Patients with a documented refusal (written or verbal) to use data for research purposes.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Return of Spontaneous Circulation (ROSC) prior to arrival of EMS.
Time frame: Time Frame: From cardiac arrest onset (as recorded by bystander/witness or dispatch log) until EMS arrival on scene (time-stamped in EMS run sheet); assessed up to 60 minutes.
Definition: Number and proportion of out-of-hospital cardiac arrest (OHCA) patients achieving ROSC prior to arrival of EMS.
Hospital admission after OHCA
Time frame: From cardiac arrest onset until documented handover at the ED or ICU (time-stamped in EMS/hospital record); assessed up to 24 hours.
Definition: Number and proportion of OHCA patients who are admitted to the hospital (survived to hand-over at the emergency department or ICU).
Occurrence of shockable rhythm at EMS arrival
Time frame: Baseline (initial rhythm documented at EMS arrival on scene).
Definition: Number and proportion of patients presenting with a shockable cardiac rhythm (ventricular fibrillation/pulseless ventricular tachycardia) upon first EMS assessment.
7 secondary outcomes
Prehospital resuscitation outcome by EMS team leadership (Emergency Physician vs Critical Care Paramedic)
Time frame: From EMS arrival on scene until hospital handover (ED/ICU) while in ROSC or death pronounced on scene; assessed up to 6 hours.
Time from Cardiac Arrest to Arrival of Organized Help
Time frame: Baseline (index OHCA event; prehospital interval, measured once).
Time to First Defibrillation
Time frame: From estimated cardiac arrest onset (witness/dispatch record) until first defibrillation (defibrillator time-stamp/EMS record); assessed up to 60 minutes.
Event Timing
Time frame: At cardiac arrest onset (baseline).
Demographics (Age, Gender)
Time frame: Baseline (at cardiac arrest onset)
Day of week of cardiac arrest occurrence
Time frame: At cardiac arrest onset (baseline)
Date and calendar distribution of cardiac arrest events
Time frame: At cardiac arrest onset (baseline)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 7 Jan 2026.
- Background: PubMed 33709992Bjornsson HM, Bjornsdottir GG, Olafsdottir H, Mogensen BA, Mogensen B, Thorgeirsson G. Effect of replacing ambulance physicians with paramedics on outcome of resuscitation for prehospital cardiac arrest. Eur J Emerg Med. 2021 Jun 1;28(3):227-232. doi: 10.1097/MEJ.0000000000000786.
- Background: PubMed 35445741Bujak K, Nadolny K, Trzeciak P, Galazkowski R, Ladny JR, Gasior M. Does the presence of physician-staffed emergency medical services improve the prognosis in out-of-hospital cardiac arrest? A propensity score matching analysis. Kardiol Pol. 2022;80(6):685-692. doi: 10.33963/KP.a2022.0109. Epub 2022 Apr 21.
- Background: PubMed 39867188Kern M, Jansen G, Strickmann B, Kerner T. Advancements in Public First Responder Programs for Out-of-Hospital Cardiac Arrest: An Updated Literature Review. Rev Cardiovasc Med. 2025 Jan 22;26(1):26140. doi: 10.31083/RCM26140. eCollection 2025 Jan.
- Background: PubMed 40250261Schwaiger D, Krosbacher A, Eckhardt C, Schausberger L, Baubin M, Rajsic S. Out-of-hospital cardiac arrest: A 10-year analysis of survival and neurological outcomes. Heart Lung. 2025 Sep-Oct;73:1-8. doi: 10.1016/j.hrtlng.2025.04.003. Epub 2025 Apr 18.
- Background: PubMed 34993887Oosterveer DM, de Visser M, Heringhaus C. Improved ROSC rates in out-of-hospital cardiac arrest patients after introduction of a text message alert system for trained volunteers. Neth Heart J. 2023 Jan;31(1):36-41. doi: 10.1007/s12471-021-01656-6. Epub 2022 Jan 6.
- Background: PubMed 35104306Oving I, de Graaf C, Masterson S, Koster RW, Zwinderman AH, Stieglis R, AliHodzic H, Baldi E, Betz S, Cimpoesu D, Folke F, Rupp D, Semeraro F, Truhlar A, Tan HL, Blom MT; ESCAPE-NET Investigators. European first responder systems and differences in return of spontaneous circulation and survival after out-of-hospital cardiac arrest: A study of registry cohorts. Lancet Reg Health Eur. 2020 Nov 20;1:100004. doi: 10.1016/j.lanepe.2020.100004. eCollection 2021 Feb.
- Background: PubMed 31430512Nehme Z, Andrew E, Bernard S, Haskins B, Smith K. Trends in survival from out-of-hospital cardiac arrests defibrillated by paramedics, first responders and bystanders. Resuscitation. 2019 Oct;143:85-91. doi: 10.1016/j.resuscitation.2019.08.018. Epub 2019 Aug 17.
- Background: PubMed 32484818Krammel M, Lobmeyr E, Sulzgruber P, Winnisch M, Weidenauer D, Poppe M, Datler P, Zeiner S, Keferboeck M, Eichelter J, Hamp T, Uray T, Schnaubelt S, Nuernberger A. The impact of a high-quality basic life support police-based first responder system on outcome after out-of-hospital cardiac arrest. PLoS One. 2020 Jun 2;15(6):e0233966. doi: 10.1371/journal.pone.0233966. eCollection 2020.
- Background: PubMed 32336582Siman-Tov M, Strugo R, Podolsky T, Rosenblat I, Blushtein O. Impact of dispatcher assisted CPR on ROSC rates: A National Cohort Study. Am J Emerg Med. 2021 Jun;44:333-338. doi: 10.1016/j.ajem.2020.04.037. Epub 2020 Apr 15.
- Background: PubMed 35257834Salhi RA, Hammond S, Lehrich JL, O'leary M, Kamdar N, Brent C, Mendes de Leon CF, Mendel P, Nelson C, Forbush B, Neumar R, Nallamothu BK, Abir M; CARES Surveillance Group. The association of fire or police first responder initiated interventions with out of hospital cardiac arrest survival. Resuscitation. 2022 May;174:9-15. doi: 10.1016/j.resuscitation.2022.02.026. Epub 2022 Mar 4.
- Individual participant dataSharing planned: No. At this time, we do not plan to share individual participant data (IPD) outside the study team due to data protection requirements and restrictions in the consent and ethics approval. Data may be available upon reasonable request to the corresponding author and subject to additional ethical approval. Ethic committee permission and strict Swiss data protection guidelines apply.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cardiac Arrest (CA) and Cardiac Arrest With Successful Resuscitation, run by Felix Brinkmann at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 7 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Return of Spontaneous Circulation (ROSC) prior to arrival of EMS. (time frame: Time Frame: From cardiac arrest onset (as recorded by bystander/witness or dispatch log) until EMS arrival on scene (time-stamped in EMS run sheet); assessed up to 60 minutes.). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07323667, which also lists 10 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Jan 2026.