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Adapted Cardiopulmonary Resuscitation Study

Adapted CPR (aCPR) a Bundle of Measures for Out of Hospital Cardiac Arrest (OHCA) Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07754656
Enrollment
216
Registered
2026-08-10
Start date
2026-01-28
Completion date
2029-03-28
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Arrest (CA)

Keywords

cardiac arrest, head up cpr, continuous adrenalin infusion, mechanical thorax compression, ITD, arterial line, diastolic blood pressure, ROSC, OHCA

Brief summary

The goal of this controlled single centre RCT is to compare frequency rates concerning return of spontaneous circulation (ROSC) in prehospital cardiac arrest. Two different algorithms (control-and interventiongroup) of advanced cardiac life support will be used to treat patients. In patients over 18 years suffering from cardiac arrest. The main question aims to answer if the frequency of ROSC differs between the groups receiving either the new Advanced Life Support (ALS) algorithm, or standard treatment. Researchers will compare the new algorithm to the standard care algorithm to see if there is a difference . Participants will be randomized to treatment on scene. The controlgroup will receive ALS standard treatment as performed in local protocols. The intervention group will receive a modified treatment including: * thorax compression via mechanical device (LUCAS 3) * head up Cardiopulmonary Resuscitation (cpr) * use of an impendance threshold device (ITD) module * arterial line placement * continuous epinephrin infusion via infusion pump * double sequence defibrillation

Interventions

PROCEDUREaCPR algorithm

* thorax compression via mechanical device (LUCAS 3) * head up cpr * use of an ITD module * arterial line placement * continuous epinephrin infusion via infusion pump * double sequence defibrillation

PROCEDUREERC ALS 2025

Placement of an IV line, placement of a supraglottic airway device or endotracheal intubation. Optional use of an intraosseus acces

Sponsors

Johannes Kepler University of Linz
Lead SponsorOTHER
Red Cross Upper Austria
CollaboratorUNKNOWN
Kepler University Hospital
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age\> 18 years * time of resuscitation \<21 minutes when enrollement starts

Exclusion criteria

* obvious pregnancy * contraindications for the use of Lucas 3 * time of resuscitation \>21 minutes and etCO2 \<15 mmHg upon arrival of the emergency physician on scene * Exclusion from the emergency physician from study due to futility.

Design outcomes

Primary

MeasureTime frameDescription
ROSCone minutefrequency of ROSC in the study cohort

Secondary

MeasureTime frameDescription
Time to ROSCPeriprocedural: from enrollement to ROSC or Termination of Resuscitation (TOR)comparison between the groups if ROSC can be achieved faster in one group
CO2Periprocedural: from enrollement to ROSC orTORMeasurement of CO2 differences between study arms
descriptive dataPeriprocedural: during study interventionanalyzing vital parameters measured

Countries

Austria

Contacts

PRINCIPAL_INVESTIGATORJens Meier, Univ. Prof.

Kepler University Hospital / Johannes Kepler University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026