PVP-Guided Decongestive Therapy in HF 2

NCT ID: NCT06495892

Last Updated: 2024-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE4

Total Enrollment

650 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-01

Study Completion Date

2026-07-01

Brief Summary

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The investigators hypothesize that a simple assessment of peripheral venous pressure (PVP) will better predict the diuretic need and long-term outcomes (all cause mortality, all cause rehospitalization, emergency department visits) compared to standard evaluation.

Detailed Description

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I. BACKGROUND AND SIGNIFICANCE

Precise assessment of volume status is essential in diagnosis and management of diuretic therapy in patients hospitalized for heart failure (HF). Unfortunately, no clear guidelines are present for in-hospital management of congestion. Consequently, nearly half of the patients hospitalized for congestive HF are discharged with persistent congestion. This contributes to high rates of readmission and mortality.

Recently, it has been shown that a simple assessment of peripheral venous pressure (PVP) demonstrates a high correlation with central venous pressure (CVP), indicating that PVP may be useful in the standard bedside clinical assessment of volume status in HF patients to help guiding decongestive therapy.

II. THE HYPOTHESIS

The main hypothesis is as follows: A simple assessment of peripheral venous pressure (PVP) will better guide the diuretic need and long-term outcomes (all-cause mortality, all cause re-hospitalization, emergency department visits) compared to standard evaluation.

III. METHODS

1. Application for Institutional Review Board (IRB)/Ethics board approval The study will be at participating centers. An IRB/Ethics board approval has been obtained from Marmara University, Pendik Training and Research Hospital local ethics board.
2. Study population Patients 18-99 years old who were admitted with a de novo or decompensated chronic HF and accept to participate in the study will be enrolled. Patients will be included regardless of ejection fraction or etiology of HF, but these will be noted as baseline variables. All patients or legal surrogate decision makers will be requested to provide a written informed consent prior to enrollment. Patients who withdraw their consent, those with upper extremity venous pathology, those with a baseline creatinine level equal to or above 3.5 mg/dL, those with severe stenotic valvular disease and hypertrophic cardiomyopathy will be excluded.
3. Data Collection The study will start at participating centers on July 1, 2024.

Baseline variables Baseline variables will be entered to the electronic study form (RedCap).

Procedures A peripheral intravenous (IV) access, using an 18 to 22-gauge IV line, will be placed preferably to an upper extremity vein before enrollment. This line will be used to draw blood samples first. After blood samples were collected the subjects will be randomized to standard or PVP guided therapy groups. Randomization will be done using a computer-generated random allocation list via RedCap randomization module. The details of demographic characteristics, symptoms, physical examination findings and drug list will be noted to a standard electronic study form (see appendix). A routine electrocardiogram and echocardiogram will be performed at the earliest convenience.

After the blood samples were collected, line will be flushed carefully. PVP will be obtained by transducing a peripheral intravenous line after zeroing at the phlebostatic axis. The phlebostatic axis will be accepted as the midpoint between the anterior and posterior surfaces of the chest at the level of the fourth intercostal space meets with sternum, which is assumed to be correlated with the mid-level of the right atrium. The patient's arm will be placed parallel to the patient such that the position of the peripheral IV to be at the phlebostatic axis. Continuity of the peripheral IV line with the central venous system will be confirmed by demonstrating augmentation of the venous pressure waveform using manual or tourniquet circumferential occlusion of the extremity proximal to the catheter and modified Valsalva maneuver. If the pressure waveform failed to augment appropriately, data will not be collected, and the patient will be documented for study purposes as a technique failure. Daily fluid intake and output, weight, and biochemistry measurements, as required, will be done.

The patients in whom the first and the predischarge PVP cannot be measured due to technical issues (unable to provide upper extremity IV access, unable to confirm augmentation or Valsalva test) will be excluded from the study. Also, the patients requiring in-hospital intubation, high-dose inotrope or vasopressor infusion (≥10 mcg.kg-1.min-1 dopamine, dobutamine or equivalent), intraaortic balloon support, dialysis or veno-venous ultrafiltration will be excluded from the study (but these patients will be included in the in-hospital analyses).

In hospital diuretic treatment will be guided by ESC guidelines (see references). In the standard therapy arm, the treatment and the decision of discharge will be left to physicians' discretion. In the PVP-guided arm, a PVP \< 9 mmHg will be targeted before discharge.

Outcomes The primary outcome of the study is the composite endpoint of all-cause mortality, all-cause hospitalization and all-cause emergency department visits. The secondary outcomes will include cardiovascular mortality, HF-related hospitalization, HF-related emergency department visits. This information on these outcomes will be obtained from the national electronic database. The follow-up duration is planned to be limited to one year.

Predefined secondary analyses

There will be subanalyses from the same cohort, as defined below:

* The correlation between predischarge PVP and long-term outcomes. A multivariable analysis will also be executed for predicting the primary end point.
* The correlation between the change in PVP during hospital stay and long-term outcomes. A multivariable analysis will also be executed for predicting the primary end point.
* The correlation between the change in PVP during hospital stay and worsening renal function, renal injury, need for dialysis or veno-venous ultrafiltration.
* The comparison of the two arms in terms of worsening renal function, need for dialysis or veno-venous ultrafiltration.
* The comparison of the two arms in terms of EVEREST congestion score.
* The comparison of the two arms in terms of the days in hospital.
* The comparison of the two arms in terms of the number of repeat hospitalizations.
* Usual patterns of diuretic use

Estimated number of subjects to be submitted:

We estimated that the enrollment of 621 participants would provide the study with a statistical power of 95% to detect a relative risk reduction of 26% (hazard ratio \[HR\] = 0.74) for the composite primary outcome (PVP-guided group: 40%, standard approach: 50%), using a two-sided test at the 0.05 significance level. This calculation assumes a 10% censoring rate and a 1-year follow-up period. The weighted event rate (πe=45%) was used to estimate the required number of events. To account for potential loss to follow-up and ensure robust analysis, the sample size was increased to 650 participants, maintaining equal allocation between groups (1:1 randomization).

Statistical Analysis Baseline characteristics will be summarized using standard descriptive statistics. Comparisons of relevant parameters between groups will be performed by chi-square, Fisher's exact test, Mann-Whitney U and student t-test, as appropriate. Kaplan-Meier analysis will be performed to determine the cumulative long-term mortality and composite outcome rates in subgroups. The mortality across groups will be compared using log-rank test. A Cox-regression model will be used to perform a survival analysis according to pre-discharge peripheral venous pressure and composite outcome. Baseline characteristics with a P value of 0.05 or less in the univariate analysis will be included and a step-down procedure will be applied for selection of final covariates. Statistical analyses will be performed with SPSS (version 24.0; SPSS Inc., Chicago, IL) and MedCalc Software (version 18.2.1 \[Evaluation version\]; MedCalc Software, Ostend, Belgium).

Conditions

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Heart Failure Congestion Congestive Heart Failure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two arms with a standard care control group and a peripheral pressure guided intervention group
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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PVP-Guided

Peripheral venous pressure guided diuretic therapy arm

Group Type EXPERIMENTAL

Diuretic therapy

Intervention Type DRUG

Diuretic therapy will be tailored according to peripheral venous pressure targets or standard approach

Control

Standard dıuretic therapy arm

Group Type ACTIVE_COMPARATOR

Diuretic therapy

Intervention Type DRUG

Diuretic therapy will be tailored according to peripheral venous pressure targets or standard approach

Interventions

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Diuretic therapy

Diuretic therapy will be tailored according to peripheral venous pressure targets or standard approach

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Hospitalization for heart failure (de novo or decompensated chronic heart failure) irrespective of left ventricular ejection fraction
* Age 18-99
* Accept to participate

Exclusion Criteria

* A prior history of upper extremity venous disease
* Serum creatinine ≥ 3.5 mg/dL
* Severe stenotic valvular disease
* Hypertrophic obstructive cardiomyopathy
* Withdrawal of consent
* Indwelling central venous catheter,
* Implanted left ventricular assist device
* History of heart transplantation
* Clinical diagnosis of cardiogenic shock
* Any right-to-left shunt
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ankara Etlik City Hospital

OTHER_GOV

Sponsor Role collaborator

Akdeniz University

OTHER

Sponsor Role collaborator

Bağcılar Training and Research Hospital

UNKNOWN

Sponsor Role collaborator

Bakırçay University, Faculty of Medicine

UNKNOWN

Sponsor Role collaborator

Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

OTHER

Sponsor Role collaborator

Eskişehir City Hospital

UNKNOWN

Sponsor Role collaborator

İdil State Hospital

UNKNOWN

Sponsor Role collaborator

Kafkas University Health Research and Application Hospital

UNKNOWN

Sponsor Role collaborator

Kutahya Health Sciences University

OTHER

Sponsor Role collaborator

Istanbul Mehmet Akif Ersoy Educational and Training Hospital

OTHER_GOV

Sponsor Role collaborator

Pazarcık State Hospital

UNKNOWN

Sponsor Role collaborator

Tokat Gaziosmanpaşa University, Faculty of Medicine

UNKNOWN

Sponsor Role collaborator

Trakya University Faculty of Medicine

UNKNOWN

Sponsor Role collaborator

Ataturk University

OTHER

Sponsor Role collaborator

Başakşehir Çam & Sakura City Hospital

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Emre K Aslanger, Prof

Role: PRINCIPAL_INVESTIGATOR

Basaksehir Pine and Sakura City Hospital

Özlem Yıldırımtürk, Prof

Role: PRINCIPAL_INVESTIGATOR

Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

Locations

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Ankara Etlik City Hospital

Ankara, , Turkey (Türkiye)

Site Status RECRUITING

Antalya Atatürk State Hospital

Antalya, , Turkey (Türkiye)

Site Status RECRUITING

Akdeniz University

Antalya, , Turkey (Türkiye)

Site Status ACTIVE_NOT_RECRUITING

Trakya University

Edirne, , Turkey (Türkiye)

Site Status RECRUITING

Erzurum Atatürk University Hospital

Erzurum, , Turkey (Türkiye)

Site Status RECRUITING

Eskişehir City Hospital

Eskişehir, , Turkey (Türkiye)

Site Status RECRUITING

Mehmet Akif Ersoy Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Basaksehir Cam and Sakura City Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Dr. Siyami Ersek Thoracic and Cardiovascular Surgery Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Bağcılar Training and Research Hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Bakırçay University, Faculty of Medicine

Izmir, , Turkey (Türkiye)

Site Status RECRUITING

Pazarcık State Hospital

Kahramanmaraş, , Turkey (Türkiye)

Site Status TERMINATED

Kafkas University Health Research and Application Hospital

Kars, , Turkey (Türkiye)

Site Status RECRUITING

Kütahya Health Sciences University

Kütahya, , Turkey (Türkiye)

Site Status RECRUITING

İdil State Hospital

Şırnak, , Turkey (Türkiye)

Site Status RECRUITING

Tokat Gaziosmanpaşa University

Tokat Province, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Emre K Aslanger, Prof

Role: CONTACT

+90 (212) 909 60 00 ext. 21067‬

Özlem Yıldırımtürk, Prof

Role: CONTACT

Facility Contacts

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Belma Kalaycı, Assoc. Prof.

Role: primary

0312 797 00 00

Çağatay Tunca, MD

Role: backup

Özgür Çağaç, MD

Role: primary

+90 242 3454550

Cihan Öztürk, Asist. Prof.

Role: primary

+90 (284) 235 76 41

Oğuzhan Birdal, Assoc. Prof.

Role: primary

+90 (442) 344 66 66

Ezgi Çamlı Babayiğit

Role: primary

+90 (222) 611 40 00

Ali K Kalkan, Prof

Role: primary

+90 (212) 692 20 00

Emre Aslanger, Prof

Role: primary

+902129096000 ext. 21067

Özlem F Pamuk, MD

Role: backup

+902129096000

Özlem Yıldırımtürk, Prof.

Role: primary

+902165424444

Esra Dönmez, MD

Role: primary

0 (212) 440 40 00

Sevgi Özcan, MD

Role: backup

0 (212) 440 40 00

Saadet Aydın, MD

Role: primary

+90(232) 493 00 00

Doğan İliş, Asist. Prof.

Role: primary

+90 (474) 225 21 06

Taner Şen, Prof

Role: primary

+90 (274) 260 00 43

Mevlüt Demir, MD

Role: backup

Barış Güven

Role: primary

+90 (486) 551 36 36

Çağrı Zorlu, Asist. Prof.

Role: primary

+90 (356) 212 95 00

References

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Mullens W, Damman K, Harjola VP, Mebazaa A, Brunner-La Rocca HP, Martens P, Testani JM, Tang WHW, Orso F, Rossignol P, Metra M, Filippatos G, Seferovic PM, Ruschitzka F, Coats AJ. The use of diuretics in heart failure with congestion - a position statement from the Heart Failure Association of the European Society of Cardiology. Eur J Heart Fail. 2019 Feb;21(2):137-155. doi: 10.1002/ejhf.1369. Epub 2019 Jan 1.

Reference Type BACKGROUND
PMID: 30600580 (View on PubMed)

Aslanger EK, Pamuk FO, Islamoglu Y, Ozates YS, Ilis D, Donmez E, Ozcan S, Babayigit EC, Demir M, Sen T, Yildirimturk O; PERIPHERAL-HF2 Investigators. Peripheral Venous Pressure-Guided Decongestive Therapy in Heart Failure 2 (PERIPHERAL-HF2). Am J Cardiol. 2025 Apr 15;241:37-42. doi: 10.1016/j.amjcard.2025.01.018. Epub 2025 Jan 22.

Reference Type DERIVED
PMID: 39855451 (View on PubMed)

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan: The main protocol

View Document

Document Type: Study Protocol: Study parameters (RedCap form printout)

View Document

Document Type: Informed Consent Form

View Document

Related Links

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https://esc365.escardio.org/presentation/263690

A preliminary study with a similar protocol from the same principal investigator (Akaslan, D., Aslanger, E., Saltan, Y., et al. Peripheral venous pressure guided decongestive therapy in HF. Eur J Heart F 2023; 125)

Other Identifiers

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BC&SSH-001

Identifier Type: -

Identifier Source: org_study_id