Clinical Trial

CTICU Device Study CRUISE

Study acronym: CRUISE
Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
The goal of this study evaluate three novel, Food and Drug Administration (FDA)-approved devices currently used to monitor blood pressure and the amount of blood that the heart pumps during each beat. These devices are the ClearSight (Edwards Life Sciences), CareTaker (CareTaker Medical) and CNAP (CNS Systems). These devices measure blood pressure, how much blood the heart is pumping around the body each minute and on a heartbeat to heartbeat basis and other parameters that can tell the doctor if the patient will benefit from specific treatments. The purpose of this study is to determine the accuracy of these devices. This knowledge will help us understand how investigators can use such non-invasive devices to care for patients at less risk than the devices currently used for such purposes. The main question the study aims to answer is: • What monitor is the most accurate in capturing non-invasive patient data?
Protocol Amendment History 6 amendments
This ClinicalTrials.gov record has been amended 6 times since 2025-02-13; most recent amendment 2026-03-04.
Status change: Not Yet Recruiting → Enrolling by Invitation 2025-07-07
Trial Details
NCT Number NCT06828432
Lead Sponsor Hernando Gomez
Collaborators: United States Department of Defense
Conditions Open Heart Surgery
Enrollment 50 participants
Start Date 2025-06-03
Primary Completion 2027-01-31 (estimated)
Study Completion 2027-01-31 (estimated)
Updated on ClinicalTrials.gov 2026-03-06