Safer heart monitoring? study tests three new devices

NCT ID NCT06828432

ENROLLING_BY_INVITATION Knowledge-focused Sponsor: Hernando Gomez Source: ClinicalTrials.gov ↗

Summary

This study aims to find out which of three FDA-approved, non-invasive monitoring devices is most accurate for tracking heart function in patients recovering from open heart surgery. Researchers will compare the devices against current standard monitors in 50 intensive care patients during the first 8 hours after their operation. The goal is to see if these newer, less invasive tools can provide reliable information to help guide patient care with lower risk.

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes NO responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for OPEN HEART SURGERY are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • University Pittsburgh Medical Center

    Pittsburgh, Pennsylvania, 15213, United States

Conditions

Explore the condition pages connected to this study.