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NEURESCUE Device as an Adjunct to In-Hospital Cardiac Arrest (ARISE) (ARISE Trial)

N/A
Recruiting
Led By David Shavelle, M.D.
Research Sponsored by neurescue
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up assessed up to 1 hour
Awards & highlights
No Placebo-Only Group

Summary

This trial tests the NEURESCUE device, a smart catheter that helps increase blood flow to the heart and brain during cardiac arrest. It is aimed at adults who need extra help beyond usual treatments. The device works by inflating a balloon in the main artery to redirect blood flow to critical areas.

Eligible Conditions
  • Cardiac Arrest
  • Cardiovascular Disease
  • Heart Attack

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~assessed up to 1 hour
This trial's timeline: 3 weeks for screening, Varies for treatment, and assessed up to 1 hour for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Secondary study objectives
Return of spontaneous circulation (ROSC)

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: TreatmentExperimental Treatment1 Intervention
The NEURESCUE device will be used as an adjunct to ACLS.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
NEURESCUE device
2022
N/A
~10

Find a Location

Who is running the clinical trial?

neurescueLead Sponsor
2 Previous Clinical Trials
10 Total Patients Enrolled
2 Trials studying Cardiac Arrest
10 Patients Enrolled for Cardiac Arrest
David Shavelle, M.D.Principal InvestigatorLong Beach Medical Center
~3 spots leftby Dec 2025