Trials / Not Yet Recruiting
Not Yet RecruitingNCT07434726
In-hospital Cardiopulmonary Resuscitation With Balloon Occlusion of the Descending Aorta
CPReboa: In-hospital Cardiopulmonary Resuscitation With Balloon Occlusion of the Descending Aorta
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 98 (estimated)
- Sponsor
- Insel Gruppe AG, University Hospital Bern · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will test if a sustained Return of Spontaneous Circulation (ROSC) in patients with cardiac arrest is more frequent when patients receive advanced cardiac life support (ACLS) alone or when they receive ACLS plus a balloon occlusion of the thoracic aorta.
Detailed description
Patients with in-hospital cardiac arrest (IHCA) outside the operating room, the coronary angiography suite and the intensive care unit (ICU) will be attended to by the hospitals resuscitation team and provided with advanced cardiac life support (ACLS) as per usual practice. A research team will be deployed simultaneously and, when patients meet inclusion criteria, will randomize patients to ACLS alone or to ACLS plus balloon occlusion of the descending thoracic aorta by means of a resuscitative endovascular occlusion of the aorta (REBOA) catheter.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | resuscitative endovascular occlusion of the aorta (REBOA) | Insertion of a balloon catheter through the common femoral artery, retrograde advancement of the catheter into the descending thoracic aorta, ballon occlusion of the aorta |
| OTHER | Advanced Cardiac Life Support (ACLS) | Advanced Cardiac Life Support (ACLS) as per American Heart Association (AHA) or European Resuscitation Council (ERC) standards |
Timeline
- Start date
- 2026-02-01
- Primary completion
- 2030-12-01
- Completion
- 2030-12-01
- First posted
- 2026-02-27
- Last updated
- 2026-02-27
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT07434726. Inclusion in this directory is not an endorsement.