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Non-invasive Venous Pressure Estimation
Sponsor: Yale University
Summary
The non-invasive central venous pressure estimation in adult cardiac intensive care units (CICU) patients study is a single-center, single-arm, investigator-blinded, interventional, intra-participant comparative, feasibility study. This study aims to assess the safety and preliminary accuracy of external jugular venous occlusion pressure measured non-invasively with the venous occlusion pressure monitoring device (CPMX2) in adult CICU patients. As a feasibility study, the primary goal is to gather preliminary data on the feasibility, safety, and effectiveness of the non-invasive CVP estimation method. Although single arm, the study will compare non-invasive CVP measurements with standard invasive CVP measurements taken concurrently. This intra-participant comparative approach is essential to validate the correlation and reliability of the non-invasive method.
Official title: Non-invasive Central Venous Pressure Estimation in Cardiac Intensive Care
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
40
Start Date
2026-01-06
Completion Date
2026-11
Last Updated
2026-01-21
Healthy Volunteers
No
Conditions
Interventions
CPMX2
Non-invasive venous occlusion pressure monitoring device
Locations (1)
Yale New Haven Hospital CICU
New Haven, Connecticut, United States