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Search / Trial NCT07020637

Assessment of Stroke Volume in Shock Using Echocardiography Versus Bioreactive Impedance

Launched by UNIVERSITY OF NEVADA, LAS VEGAS · Jun 5, 2025

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Cheeta Nicom Bioreactance Transthoracic Echocardiography Passive Leg Raising Stroke Volume Shock Assssment Noninvasive Cardiac Output Monitoring

ClinConnect Summary

This clinical trial is studying two different methods to measure stroke volume, which is the amount of blood the heart pumps with each beat, in patients who are experiencing shock—a serious condition where the body doesn't get enough blood flow. The researchers want to see how closely the results from echocardiography (a test that uses sound waves to create images of the heart) match up with another non-invasive method called bioreactance. This study is important because accurate measurements can help doctors make better decisions about treating critically ill patients.

To participate in this trial, you need to be an adult aged 18 or older and have a clinical diagnosis of shock, such as low blood pressure that requires medication. You also need to be able to give consent or have someone legally authorized to give consent for you. However, if you are pregnant, have severe heart valve disease, or certain other health conditions, you would not be eligible. If you join the trial, you can expect to undergo both types of tests to measure your heart's function, which could help improve care for patients in similar situations in the future.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • 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
  • Exclusion Criteria:
  • 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

About University Of Nevada, Las Vegas

The University of Nevada, Las Vegas (UNLV) is a prominent research institution committed to advancing healthcare through innovative clinical trials. With a focus on multidisciplinary collaboration, UNLV engages in rigorous scientific inquiry to explore new treatments and interventions that address pressing health challenges. The university's dedicated faculty and state-of-the-art facilities foster an environment conducive to cutting-edge research, ensuring the highest standards of ethical practice and patient care. Through its clinical trials, UNLV aims to contribute to the body of medical knowledge while improving health outcomes for diverse populations.

Locations

Las Vegas, Nevada, United States

Patients applied

0 patients applied

Trial Officials

Mutsumi J Kioka, Medical Doctor

Principal Investigator

UNLV

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported