EICHORCondition: Cardiac Intensive Care · Sponsor: Yale University
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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.
This description comes directly from the study's public registry record.
Elliott Miller, MD, MS · 203-737-6390 · elliott.miller@yale.edu
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| Yale New Haven Hospital CICU | New Haven, Connecticut, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07226479