Peripheral Venous Pressure (PVP) Trial

Part of paid clinical trials in Milwaukee, Wisconsin.

Sponsor
Wake Forest University Health Sciences
Study ID
NCT07400042
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • 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.
  • standard clinical care — OTHER
    Usual standard clinical care

Study Details

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.

Key Dates

First listed
Feb 10, 2026
Start date
Jul 27, 2026
Status verified
Aug 2026
Primary completion
Aug 31, 2031
Completion
Aug 31, 2031

Study Design

Enrollment
600 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: peripheral venous pressure measurements
    Peripheral venous pressure measures provided to physicians daily up to 8 days
  • Active Comparator: standard clinical care
    Usual standard clinical care, peripheral venous pressure measures not provided to physician daily

Primary Outcome Measure

Length of hospital stay [ Time Frame: up to day 8 ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Aurora St. Luke's Medical CenterMilwaukeeWisconsin53215
Khawaja A Ammar, MD
414-649-6181

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