Assessment of Stroke Volume in Shock Using Echocardiography Versus Bioreactive Impedance

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorUniversity of Nevada, Las Vegas

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 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

Disqualifiers

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)

Trial population

Adult patients admitted to the intensive care unit (ICU) with clinical signs of shock, including hypotension and/or evidence of end-organ hypoperfusion, who are able to provide informed consent or have a legally authorized representative available.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Cheetah NICOM

    Device

    Bioreactance-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.

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Shock Patients1 intervention

Trial outcomes

Primary outcomes

1

Correlation Between Stroke Volume Measurements by Echocardiography and Bioreactance Monitoring

Pearson correlation coefficient between stroke volume measurements obtained using transthoracic echocardiography and those obtained using bioreactance-based monitoring (Cheetah NICOM) in response to passive leg raising.

Time frame
Within 1 hour of enrollment

Secondary outcomes

Other outcomes

Sponsors and contacts

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