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RECRUITING
NCT07226479
NA

Non-invasive Venous Pressure Estimation

Sponsor: Yale University

View on ClinicalTrials.gov

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

Interventions

DEVICE

CPMX2

Non-invasive venous occlusion pressure monitoring device

Locations (1)

Yale New Haven Hospital CICU

New Haven, Connecticut, United States