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.
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