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Tolvaptan/Ultrafiltration in the Treatment of Acute Heart Failure

Primary Mode of Therapy in Acute Decompensated Heart Failure:Comparison Between Usual Care Plus Tolvaptan and Ultrafiltration.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01863511
Acronym
TUF
Enrollment
45
Registered
2013-05-29
Start date
2013-05-31
Completion date
2015-12-31
Last updated
2016-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Decompensated Heart Failure

Keywords

Treatment options for acute decompensated heart failure, Ultrafiltration, tolvaptan

Brief summary

For patients hospitalized with acute decompensated heart failure,volume removal remains the primary therapeutic objective. The current standard of care remains loop diuretics.The high likelihood of readmissions and poor outcomes highlights the need to examine and improve in-hospital protocols for these patients. Ultrafiltration allows for greater volume removal, less neurohormonal stimulation and greater sodium removal.However it is associated with increased costs, line complications, and relative immobility during treatment. Tolvaptan in addition to diuretic therapy has been shown to improve the amount of volume removed compared to diuretic alone. The study proposes to compare the strategy of adding tolvaptan to usual care with ultrafiltration as primary mode of therapy in acute decompensated HF(ADHF) patients. Hypothesis: addition of tolvaptan to usual care for hospitalized HF patients will result in: * greater volume and weight reduction compared with usual care * similar efficacy outcomes compared with ultrafiltration, with less complications of therapy

Detailed description

Study design is a prospective randomized open labeled and unblinded comparison of two different approaches to volume removal. Enrolled patients will be evaluated for target weight to be removed. Patients will be randomized to usual care (UC), usual care plus tolvaptan (UC+T) or ultrafiltration (UF), within 12 hours of presentation. Treatment in the UC and UC+T arms will begin with a furosemide bolus(double the home dose or if unavailable, 60mg) and continue with a drip(10 or 20 mg/hr). In addition the UC+T group will be treated with tolvaptan 30 mg orally once daily. Patients in the UF arm will be treated with UF administered through a brachial line or a catheter in the internal jugular vein. Loop and thiazide diuretics will be discontinued, although aldosterole antagonists will be continued. Urinary neutrophil gelatinase associated lipocalcin(uNGAL)levels are elevated in renal dysfunction and may be a sensitive biomarker to distinguish between intrinsic renal damage and reversible, transient prerenal azotemia.Characterizing the changes in uNGAL levels during the course of ADHF therapy, in comparison with patient weight, BUN and creatinine levels is an important step in establishing the role of this potential promising biomarker in ADHF treatment strategies. Protocol highlights for all patients include: Baseline labs and daily through day 4 and at discharge(BMP, BNP, CBC, urine creatinine and sodium, uNGAL) * Daily am weights * Daily volume status:total intake, urine output, ultrafiltrate volume * Collect all urine and ultrafiltrate in a 24 hour collection bag, record volume, creatinine and Na levels * length of stay * hospital day 4: Minnesota Living with Heart Failure questionnaire * Cost of hospitalization

Interventions

DRUGloop diuretic
DRUGtolvaptan

Sponsors

The Christ Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 2 of 3 physical exam findings of volume overload (rales, JVP over 5 cm and edema) * BNP over 300 * no contraindication to ultrafiltration (line insertion, heparin use)

Exclusion criteria

* serum creatinine \> 3mg/dL or Na \> 145 * inotrope or vasopressor dependency * active infection, including urinary tract * resynchronization therapy or coronary intervention in past 30 days * life expectancy less than 6 months * hypertrophic obstructive cardiomyopathy with peak resting gradient \> 20 mmHg * IV contrast or NSAID use in the past 1 week (uNGAL related requirement)

Design outcomes

Primary

MeasureTime frame
Net change in weightday 1,2,3,4,5

Secondary

MeasureTime frame
net volume lossday 1,2,3,4,5
urinary NGALDay 1,2,3,4,5
dyspnea scorebaseline and day 5
BNP change from admission to dischargebaseline and day 5
serum creatinine changeDay 1,2,3,4,5
all cause readmission30 day
all cause death30 day
serum sodium and potassium changesbaseline through day 5
Quality of Lifeday 4 of hospital stay

Other

MeasureTime frame
nursing intensityday 1,2,3,4,5
peripheral vs. central access, number of filters used, complications of heparin useday 1,2,3,4,5

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026