Vein pressure check could slash hospital stays for heart failure patients
NCT ID NCT07400042
First seen Jun 24, 2026 · Last updated Aug 28, 2026 · Updated 5 times
Summary
This study tests whether giving doctors daily readings of a patient's peripheral venous pressure (a simple vein pressure measurement) can help heart failure patients get out of the hospital faster and avoid coming back. Researchers will compare 600 patients who get this extra information with those who receive standard care. The goal is to see if this easy-to-do test can improve hospital management and reduce repeat hospitalizations.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- peripheral venous pressure measurement
- What this could lead to
- If successful, this could give doctors a simple, non-invasive tool to better manage heart failure patients in the hospital, potentially reducing time in the hospital and repeat visits.
- What could go wrong
- This is an early-stage study with no phase, and the intervention is only a measurement—not a treatment. It may not significantly change outcomes, and results may not apply to all heart failure patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 600 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Aug 2031
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with minimum 3-month history of Congestive Heart Failure admitted to Aurora St. Luke's Medical Center with acute decompensation * English speaking only Exclusion Criteria: * Patients who do not already have a peripheral IV line inserted * Patients whose IV line cannot be transduced * Patients with current or past vein thrombosis in the arm used to measure the pressure or with history of recurrent (\>1) pulmonary embolism * Patients with active thrombophlebitis in the arm * Patients who have experienced a major cardiovascular event (myocardial infarction, stroke, etc.) ≤2 months prior to the admission date * Patients who have received an implanted cardiac resynchronization device (pacemaker or ICD) ≤3 months prior to admission date * Patients enrolled in other cardiovascular research studies. * Patients with a clinical condition that the investigator believes may not allow the patient to complete the study, at the discretion of the investigator. Examples of conditions that may apply include severe stenotic valvular disease, isolated right ventricle failure, precapillary pulmonary hypertension, hypertrophic obstructive cardiomyopathy, implanted left ventricular assist device, history of heart transplantation, clinical diagnosis of cardiogenic shock, any left-to-right shunt * Patients with congenital heart disease or mechanical right heart valve(s) * Planned heart surgery and/or coronary intervention during hospitalization * Patients expected to receive heart transplant within 6 months of admission * IV cannula smaller than 22G * Patients who are pregnant and/or lactating * Patients who are unable to provide informed consent * Patients who are intubated
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Aurora St. Luke's Medical Center
RECRUITINGMilwaukee, Wisconsin, 53215, United States
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