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RecruitingNCT07400042Updated Oct 7, 2026

Peripheral Venous Pressure (PVP) Trial

An interventional study of peripheral venous pressure measurements and standard clinical care in Congestive Heart Failure, sponsored by Wake Forest University Health Sciences. Recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-07.

Sponsored by Wake Forest University Health Sciences · Not applicable, Interventional, and Treatment

Updated Oct 7, 2026Start date movedPrimary completion moved+1 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

The objective of the study is to evaluate the effectiveness of standard clinical care versus standard clinical care directed by peripheral venous pressure on length of hospital stay and incidence of rehospitalization among heart failure patients.

The study team hypothesizes that compared to standard clinical care the peripheral venous pressure-guided therapy is associated with shorter hospital stay and lesser incidence of 30-day rehospitalization. The study team will also collect data to determine if peripheral venous pressure-guided care is associated with reduced incidence of 6-month rehospitalization, improvement in symptoms or lab indices, lesser new incidence of dialysis, change in use of diuretics, and lesser use of echocardiograms.

02

Conditions studied

  • Congestive Heart Failure

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Keywords

  • peripheral venous pressure
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's planned enrollment of 600 is above the median of 72 across 3,736 interventional studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

Wake Forest University Health Sciences is the lead sponsor of 1,320 studies on the registry; 199 are open to participants now.

Of its 323 completed or terminated interventional studies of FDA-regulated products, 243 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    peripheral venous pressure measurements

    Peripheral venous pressure measures provided to physicians daily up to 8 days

    Other: peripheral venous pressure measurements

  • Active comparator
    standard clinical care

    Usual standard clinical care, peripheral venous pressure measures not provided to physician daily

    Other: standard clinical care

Interventions

  • Otherperipheral venous pressure measurements

    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.

  • Otherstandard clinical care

    Usual standard clinical care

06

What researchers measure

Primary outcomes

  1. Length of hospital stay

    Number of days from admission to discharge

    Time frame: up to day 8

  2. Number of subjects rehospitalized

    Number of subjects in each group who have been rehospitalized

    Time frame: Day 30 post index hospitalization

  3. Number of subjects rehospitalized

    Number of subjects in each group who have been rehospitalized

    Time frame: Month 6 post index hospitalization

Secondary outcomes

  1. Number of subjects with exertional dyspnea

    Number of subjects in each group experiencing dyspnea according to the New York Heart Association Class

    Time frame: Day 1 and date of discharge (up to day 8)

  2. Number of subjects with exertional orthopnea

    Number of subjects in each group experiencing orthopnea according to the New York Heart Association Class

    Time frame: Day 1 and date of discharge (up to day 8)

  3. Number of subjects with new need for dialysis during index hospitalization

    Number of subjects in each group with new need for dialysis during index hospitalization

    Time frame: Day 1 and date of discharge (up to day 8)

  4. Number of subjects with diuretic use

    Number of subjects in each group with diuretic use during index hospitalization

    Time frame: Day 1 and date of discharge (up to day 8)

  5. Number of subjects with echocardiograms

    Number of subjects in each group with echocardiograms performed (with results) during index hospitalization

    Time frame: Day 1 and date of discharge (up to day 8)

  6. Number of subjects with all-cause death

    Number of subjects in each group with all-cause death

    Time frame: Month 6 post index hospitalization

  7. Number of subjects with cardiac-related death

    Number of subjects in each group with cardiac-related death

    Time frame: Month 6 post index hospitalization

07

Study locations

1 of 1 sites recruiting
  • Aurora St. Luke's Medical Center
    Milwaukee, Wisconsin 53215, United States
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Start date
Jul 27, 2026→Oct 5, 2026
Oct 7, 2026
Primary completion
Aug 2031→Oct 2031
Oct 7, 2026
Study completion
Aug 2031→Oct 2031
Oct 7, 2026
Show all 1 update
  1. Oct 7, 2026
    Start date Jul 27, 2026→Oct 5, 2026
    Primary completion Aug 2031→Oct 2031
    Study completion Aug 2031→Oct 2031

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07400042
Lead sponsor
Wake Forest University Health Sciences
Responsible party
Sponsor
First posted
Feb 10, 2026
Start date
Oct 5, 2026
Primary completion
Oct 2031 (estimated)
Completion
Oct 2031 (estimated)
Last update
Oct 7, 2026

Study contacts

Khawaja Ammar, MD
Contact
Khawaja.Ammar@aah.org
(414) 649-6181
Khawaja Ammar, MD
principal investigator · Wake Forest University Health Sciences

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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