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Clinical Trial

Non-invasive Venous Pressure Estimation

NCT: NCT07226479 · RECRUITING

NCT IDNCT07226479
StatusRECRUITING
Start Date2026-01-06
SponsorYale University (OTHER)
First posted
Last updated

Brief 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 Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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