Peripheral Venous Pressure (PVP) Trial
Sponsor: Wake Forest University Health Sciences • ClinicalTrials.gov ID: NCT07400042
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The purpose of the study is to determine if there is a reduction in the length of stay and rates of rehospitalization for patients diagnosed with congestive heart failure when physicians are provided daily measurements of peripheral venous pressure versus no daily measurements of peripheral venous pressure.
Interventions
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peripheral venous pressure measurements
(Other)
Peripheral venous pressure measures provided to physicians daily up to 8 days, with a research note in the electronic medical record containing standardized recommendations for case also provided daily. Care changes up to clinical provider discretion.
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standard clinical care
(Other)
Usual standard clinical care
Eligibility criteria
Conditions
Locations
- Aurora St. Luke's Medical Center — Milwaukee, Wisconsin, United States
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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