Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07434726

In-hospital Cardiopulmonary Resuscitation With Balloon Occlusion of the Descending Aorta

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2026-04-23

98

Participants Needed

1

Research Sites

241 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

In-hospital Cardiopulmonary Resuscitation With Balloon Occlusion of the Descending Aorta

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients suffering from in-hospital cardiac arrest (IHCA), including those with out-of-hospital cardiac arrest (OHCA) and return of spontaneous circulation (ROSC) transported to the emergency department who then suffer a second arrest
  • Successful placement of a femoral artery introducer sheath
  • Any electrical cardiac activity seen in the initial rhythm analysis
  • Ongoing effort of resuscitation as determined by a study-independent resuscitation lead
Not Eligible

You will not qualify if you...

  • IHCA occurring in the operating room, intensive care unit, or cardiac catheter laboratory
  • Hospital visitors suffering from cardiac arrest
  • Asystole seen in the initial rhythm analysis
  • Presumed age under 18 years
  • Known "do not resuscitate" order
  • Known or obvious pregnancy
  • Traumatic cardiac arrest
  • Known aortic pathologies that prevent cannulation
  • Known allergies to radiographic contrast agents

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Inselspital University Hospital Bern

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

W

Wolf E Hautz, MD, MME

CONTACT

C

Cornelia Lammbrigger, RN

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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