Cardiac Arrest Clinical Trials

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A Randomized Controlled Study of the NEURESCUE Device as an Adjunct to Advanced Cardiac Life Support

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure, Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The NEURESCUE device is the first intelligent balloon catheter for aortic balloon occlusion (ABO), an emergency technique that supercharges blood flow to the heart and brain within one minute from deployment. The catheter-based device is delivered via the femoral artery, temporarily inflating a soft balloon in the descending to redirect blood flow towards the upper body. The purpose of this study is to compare the clinical safety and performance of Advanced Cardiovascular Life Support (ACLS) versus ACLS in combination with Aortic Balloon Occlusion (ABO) using the NEURESCUE device in subjects with cardiac arrest.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Age ≥18 and ≤80 years

• Witnessed arrest

• CPR initiated within 7 min of arrest

• CPR time less than 40 min at enrollment

• Non-shockable rhythm

Locations
Other Locations
Germany
Charité - Universitätsklinikum Berlin
RECRUITING
Berlin
University Hospital Heidelberg
RECRUITING
Heidelberg
Contact Information
Primary
Michael Preusch, M.D.
Michael.Preusch@med.uni-heidelberg.de
+49 151 40044669‬
Time Frame
Start Date: 2025-07-07
Estimated Completion Date: 2027-03
Participants
Target number of participants: 84
Treatments
Active_comparator: Arm 1 (Control)
Enrolled subjects randomized into Arm 1 will receive ACLS treatment.
Experimental: Arm 2 (Intervention)
Enrolled subjects randomized into Arm 2 will receive ACLS treatment combined with ABO.
Related Therapeutic Areas
Sponsors
Leads: neurescue

This content was sourced from clinicaltrials.gov