Assessment of Stroke Volume in Shock Using Echocardiography Versus Bioreactive Impedance
Part of paid clinical trials in Las Vegas, Nevada.
- Sponsor
- University of Nevada, Las Vegas
- Study ID
- NCT07020637
- Status
- Recruiting
Conditions
- Critical Illness
- Shock
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Cheetah NICOM — DEVICEBioreactance-based noninvasive cardiac output monitoring device used to measure stroke volume before and after passive leg raising. Used solely for observational measurement. No therapeutic intervention is performed.
Study Details
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.
Key Dates
- Start date
- Oct 19, 2024
- Status verified
- Apr 2026
- Primary completion
- Apr 30, 2026
- Completion
- Apr 30, 2026
Study Design
- Enrollment
- 30 participants (estimated)
Arms
- Arm: Shock PatientsThis cohort includes adult patients presenting with clinical signs of shock in the intensive care unit. Each participant will undergo stroke volume measurement using both transthoracic echocardiography and bioreactance-based monitoring (Cheetah NICOM) before and after passive leg raising. No therapeutic intervention will be performed as part of the study.
Primary Outcome Measure
Correlation Between Stroke Volume Measurements by Echocardiography and Bioreactance Monitoring [ Time Frame: Within 1 hour of enrollment ]
Central Contacts
- Mutsumi J Kioka, Medical Doctor7026712345
- Office of Research Integrity Human Subjects UNLV7028952794
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University Medical Center Southern Nevada | Las Vegas | Nevada | 89102 |
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