Non-invasive Venous Pressure Estimation

Recruiting N/A Interventional Study
Cardiac Intensive Care
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Device Feasibility
Participants needed
40 (estimated)
Sponsor
Yale University · Other
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About This Trial
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 m…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Provision of signed and dated informed consent * Admitted to the CICU with invasive CVP/RA pressure monitoring placed by standard of care as determined by the treating team before enrollment * No more than moderate TR as assessed by echocardiogram Exclusion Criteria: * Under…
Contacts

Elliott Miller, MD, MS

203-737-6390

elliott.miller@yale.edu

CONTACT