The Application of Positive End-Expiratory Pressure in Out-of-Hospital Cardiac Arrest: The Lazarus-PEEP Trial.

NCT ID: NCT06939335

Last Updated: 2026-01-21

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 132 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-04-25
• Study Completion Date: 2027-02-01

Brief Summary

The goal of this clinical trial is to learn whether using Positive End-Expiratory Pressure (PEEP) during cardiopulmonary resuscitation (CPR) improves outcomes for adults who experience out-of-hospital cardiac arrest, a condition where the heart suddenly stops beating. PEEP is used during ventilation, which may enhance oxygen levels by keeping the airways open throughout CPR.

This study aims to determine if using PEEP during CPR helps restart the heart more effectively, improves survival rates, and enhances survival with good neurologic outcomes after a cardiac arrest compared to standard CPR without PEEP.

Researchers will randomly assign participants to one of two groups: one receiving CPR with PEEP set at 5 cm of water pressure and the other receiving standard CPR without PEEP. Participants will be treated by emergency medical teams trained in advanced life support, and specialised sensors will measure airflow and airway pressure during resuscitation.

Additionally, the study will evaluate potential side effects associated with PEEP, such as increased pressure within the chest or lung injuries. Findings from this trial will guide recommendations on the usage of PEEP in standard CPR practices to potentially improve patient outcomes.

Detailed Description

Introduction: Sudden cardiac arrest is a significant cause of mortality, with an estimated annual incidence of 84 cases per 100,000 individuals in Europe. Effective cardiopulmonary resuscitation (CPR), including proper ventilation, is crucial for survival. However, the interplay between ventilation and circulation during CPR is complex and not fully understood. While ventilation is necessary for oxygenation, excessive hyperventilation and high intrathoracic pressures can be detrimental. Positive End-Expiratory Pressure (PEEP) may improve oxygenation and ventilation by maintaining alveolar patency and improving oxygenation. Previous observational studies have suggested that PEEP might enhance the rate of Return of Spontaneous Circulation (ROSC) and improve short-term outcomes. However, no prospective randomised clinical trials have been conducted to confirm these findings. The Lazarus-PEEP trial aims to address this gap by evaluating the efficacy and safety of PEEP during CPR for out-of-hospital cardiac arrest (OHCA) patients.

Methodology: The study will be conducted at Ghent University Hospital and three non-university hospitals in Belgium, enrolling adult patients who experience non-traumatic OHCA and are intubated and ventilated during resuscitation efforts by an advanced life support (MUG) team. Participants will be randomised to receive either PEEP at 5 cm H2O or no PEEP (0 cm H2O) during CPR. Custom-built sensors will measure tracheal airflow and pressure, while additional data on CPR quality and patient outcomes will be collected. The trial's primary outcome measure is the rate of ROSC, with secondary outcomes including survival to hospital admission and discharge, as well as neurological outcomes at discharge.

Outcome: The study will evaluate the effectiveness of PEEP in improving ROSC rates, short-term survival, and neurological outcomes. Safety profiles will also be examined, focusing on adverse effects such as barotrauma and increased intrathoracic pressures. Comprehensive data collection will provide insights into the physiological impact of PEEP during CPR and its feasibility in a pre-hospital setting.

Conclusion: The Lazarus-PEEP trial aims to gather strong evidence on the potential advantages and risks of utilizing PEEP during CPR for OHCA patients. The results will inform evidence-based guidelines and enhance resuscitation practices, potentially leading to improved patient outcomes. The findings will be disseminated through influential journals, major scientific conferences, and public data-sharing platforms to ensure widespread accessibility and impact.

Conditions

Cardiac Arrest (CA); Out-of-hospital Cardiac Arrest (OHCA); Positive End-expiratory Pressure (PEEP); Ventilation During Resuscitation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Intervention

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 and a disposable PEEP Valve set at 5 cm H20.

Group Type: EXPERIMENTAL

Disposable PEEP Valve set at 5 cm H20.

Intervention Type: DEVICE

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 and a 22 mm disposable PEEP Valve set at 5 cm H20.

Controle

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 without a disposable PEEP Valve.

Group Type: ACTIVE_COMPARATOR

Controle

Intervention Type: DEVICE

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 without a disposable PEEP Valve.

Interventions

Disposable PEEP Valve set at 5 cm H20.

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 and a 22 mm disposable PEEP Valve set at 5 cm H20.

Intervention Type: DEVICE

Controle

Ventilation during cardiac arrest with an adult Resuscitation Bag with a pressure relief valve set at 40 cm H20 without a disposable PEEP Valve.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Age: Adults aged 18 years and older.

2. Type of Cardiac Arrest: Patients who have experienced a non-traumatic out-of-hospital cardiac arrest.

3. CPR Administration: Patients receiving cardiopulmonary resuscitation from an advanced life support (ALS) team.

4. Intubation and Ventilation: Patients who are intubated and ventilated during resuscitation efforts.

Exclusion Criteria

1. Cardiac arrest in patient younger than 18 years of age.

2. Traumatic cardiac arrest, including drowning, penetrating or blunt injury, and burns.

3. Immediate Return of Spontaneous Circulation (ROSC): Patients who achieve ROSC before intubation and initiation of intubation.

4. Pregnancy.

5. Mechanical ventilation during arrest: patients already receiving mechanical ventilation at the moment of cardiac arrest, due to reasons other than their arrest, will be excluded.

6. Do Not Resuscitate (DNR) Orders: Patients with existing DNR orders or any advanced directive indicating that CPR should not be performed.

7. Failure to intubate: if intubation is unsuccessful, ventilation by any means (MBV, SGA) should take priority over the study protocol, and the patient is excluded.

8. Enrolment in Other Studies: Patients currently enrolled in another interventional clinical trial that could interfere with the outcomes of this study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Ghent

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Saïd Hachimi Idrissi, MD, PhD, Professor

Role: PRINCIPAL_INVESTIGATOR

UZ Gent

Locations

AZ Oostende

Ostend, West-Flandres, Belgium

Site Status: RECRUITING

AZORG: campus Merestraat

Aalst, , Belgium

Site Status: RECRUITING

AZORG: Campus Moorselbaan

Aalst, , Belgium

Site Status: RECRUITING

AZORG: campus Geraardsbergen

Geraardsbergen, , Belgium

Site Status: RECRUITING

UZ Ghent

Ghent, , Belgium

Site Status: RECRUITING

AZ Zeno

Knokke, , Belgium

Site Status: RECRUITING

Centre hospitalier universitaire (CHU) Besançon-Franche-Comté

Besançon, , France

Site Status: ACTIVE_NOT_RECRUITING

Countries

Belgium; France

Central Contacts

Thomas Tackaert, MD

Role: CONTACT

thomas.tackaert@ugent.be

0032 53 72 49 96

Facility Contacts

Maxim Vanwulpen, MD, PhD

Role: primary

maxim.vanwulpen@azoostende.be

0032 59 41 40 80

AZORG: campus Merestraat

Role: primary

spoedopname.asz@azorg.be

0032 53 76 40 06

AZORG: Campus Moorselbaan

Role: primary

0032 53 72 49 96

AZORG: campus Geraardsbergen

Role: primary

spoedopname@azorg.be

0032 54 43 27 11

Spoedgevallendienst UZ Gent

Role: primary

secretariaatspoed@uzgent.be

0032 9 332 50 24

Urgentiegeneeskunde - spoed AZ Zeno Knokke-Heist

Role: primary

info@azzeno.be

0032 50 535 112

Other Identifiers

ONZ-2024-0496

Identifier Type: -

Identifier Source: org_study_id