Actively Recruiting

Age: 18Years - 90Years
All Genders
NCT07020637

Assessment of Stroke Volume in Shock Using Echocardiography Versus Bioreactive Impedance

Led by University of Nevada, Las Vegas · Updated on 2026-04-15

30

Participants Needed

1

Research Sites

79 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the correlation between stroke volume measurements obtained by transthoracic echocardiography and bioreactance-based noninvasive cardiac output monitoring. The primary objective is to assess the level of agreement between these two modalities in critically ill patients.

CONDITIONS

Official Title

Assessment of Stroke Volume in Shock Using Echocardiography Versus Bioreactive Impedance

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 218 years
  • Clinical diagnosis of shock as determined by the treating ICU physician (e.g., hypotension requiring vasopressors or evidence of end-organ hypoperfusion)
  • Able to obtain informed consent from the patient or a legally authorized representative
  • Enrollment within 24 hours of ICU admission
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Known severe aortic valve disease or dynamic left ventricular outflow tract obstruction
  • Morbid obesity (BMI > 40) that precludes accurate echocardiographic imaging
  • Presence of cardiac arrhythmias (e.g., atrial fibrillation with rapid ventricular response) affecting stroke volume measurements
  • Implanted cardiac assist devices (e.g., LVAD, pacemaker dependency)
  • Imminent death or decision for comfort care only

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

University Medical Center Southern Nevada

Las Vegas, Nevada, United States, 89102

Actively Recruiting

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Research Team

M

Mutsumi J Kioka, Medical Doctor

CONTACT

O

Office of Research Integrity Human Subjects UNLV

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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