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RHAPSody: Diagnostic Utility of RUSH Following ROSC

NCT03409289 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 5

Last updated 2022-12-27

No results posted yet for this study

Summary

This will be a prospective observational study of adult primary cardiac arrest patients presenting to Shands Emergency Department following ROSC or actively in cardiac arrest with subsequent ROSC after treatment in the emergency department.

Conditions

  • Cardiac Arrest

Interventions

DEVICE

RUSH Exam

Within two hours of return of spontaneous circulation, the following elements of the RUSH exam will be performed: focused evaluation of the heart, inferior vena cava, abdomen and aorta with the addition of evaluation for DVT and ocular ultrasound.

Sponsors & Collaborators

  • University of Florida

    lead OTHER

Principal Investigators

  • Leslie C. Nickels, MD · University of Florida

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2020-11-14
Completion
2020-11-14
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03409289 on ClinicalTrials.gov