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Clinical Trials/NCT01474200
NCT01474200
Terminated
Not Applicable

Aquapheresis Versus Intravenous Diuretics and Hospitalizations for Heart Failure (AVOID-HF)

Nuwellis, Inc.38 sites in 1 country224 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Isolated veno-venous ultrafiltration (AQ)
Conditions
Heart Failure
Sponsor
Nuwellis, Inc.
Enrollment
224
Locations
38
Primary Endpoint
Time to First Heart Failure (HF) Event
Status
Terminated
Last Updated
2 years ago

Overview

Brief Summary

The purpose of the research is to determine if patients have fewer Heart Failure (HF) events after receiving Aquapheresis (AQ) therapy compared to intravenous (IV) diuretics up to 90 days of discharge from the hospital. Heart Failure events are defined as returning to the hospital, clinic or emergency department (ED) for treatment of HF symptoms.

Detailed Description

The aim of the proposed AVOID-HF study is to confirm and expand the findings that fluid removal by AQ reduces HF rehospitalizations at 90 days as well as the length of these HF rehospitalizations. In the "Ultrafiltration Versus Intravenous Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure" (UNLOAD) study, the 90 day HF re-hospitalizations were pre-specified secondary end-points. AVOID-HF is designed with a primary end-point to determine if AQ reduces the number of HF events (Rehospitalization or unscheduled outpatient or emergency room treatment for HF) after discharge from index hospitalization compared to IV loop diuretics. AVOID will also explore days alive and out of the hospital as a secondary end-point, which was not done in UNLOAD. In other words, the AVOID-HF study is going beyond studying only the amount of fluid removal and will explore whether the modality of fluid removal influences HF outcomes.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
July 2014
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or older
  • Male or non-pregnant female patients
  • Admitted to the hospital with a primary diagnosis of acute decompensated heart failure (ADHF)
  • On regularly scheduled oral loop diuretics prior to admission
  • Fluid overload manifested by at least two of the following:
  • Pitting edema (2+) of the lower extremities
  • Jugular venous distention \> 8 cm
  • Pulmonary edema or pleural effusion on chest x-ray
  • Paroxysmal nocturnal dyspnea or ≥ two- pillow orthopnea
  • Respiration rate ≥ 20 per minute.

Exclusion Criteria

  • Acute coronary syndromes
  • Renal insufficiency with a sCr ≥ 3.0 mg/dl or planned renal replacement therapies
  • Systolic blood pressure \< 90 mmHg at time of enrollment
  • Pulmonary Arterial Hypertension not secondary to left heart disease
  • Contraindications to systemic anticoagulation
  • Hematocrit \> 45%
  • Inability to obtain venous access
  • Hemodynamic instability severe enough to require IV positive inotropic agents, IV vasodilators or both
  • Use of iodinated radiocontrast material within the previous 72 hours or planned study requiring IV contrast during the current hospitalization
  • Severe concomitant disease expected to prolong hospitalization

Arms & Interventions

Aquapheresis (AQ) - isolated veno-venous ultrafiltration

Excess fluid from the patient is removed by isolated veno-venous ultrafiltration treatment using the Aquadex Flex Flow System

Intervention: Isolated veno-venous ultrafiltration (AQ)

IV Loop Diuretics (LD)

Excess fluid from the patient is removed by IV (Intravenous) loop diuretic treatment

Intervention: IV Loop Diuretics (LD)

Outcomes

Primary Outcomes

Time to First Heart Failure (HF) Event

Time Frame: 90 days after discharge from index HF hospitalization.

Time to first HF event within 90 days after discharge from index HF hospitalization. HF events are defined as * HF rehospitalization or * unscheduled outpatient or emergency room treatment with IV loop diuretics or * unscheduled outpatient Aquapheresis treatment

Secondary Outcomes

  • CLINICAL: Total Number of Cardiovascular (CV) Rehospitalizations at 30 and 90 Days After Discharge(Within 30 days and 90 days after hospital discharge)
  • EFFICACY: Net Fluid Removed During the Index Hospitalization(Index Hospitalization, an average of 8 days)
  • EFFICACY: Total Fluid Removed During the Index Hospitalization(Index Hospitalization, an average of 8 days)
  • EFFICACY: Changes in B-type Natriuretic Peptide (BNP) Levels Over Time(Baseline and at 72 hours from baseline, hospital discharge and at 90 days after hospital discharge)
  • EFFICACY: Weight Loss at 72 Hours After Initiation of Treatment(72 hours after treatment initiation)
  • Length of Stay (LOS) During the Index Hospitalization(Index hospitalization admission to index hospitalization discharge)
  • CLINICAL: Total Number of Emergency Department (ED) or Unscheduled Office Visits at 30 and 90 Days After Discharge(Within 30 days and 90 days after hospital discharge)
  • Quality of Life Assessed Using the Kansas City Cardiomyopathy Questionnaire (KCCQ) at 30, 60 and 90 Days After Discharge(Within 90 days after hospital discharge)
  • SAFETY: Changes in Renal Function (Serum Creatinine) After Treatment up to 90 Days After Randomization(Within 90 days of randomization)
  • SAFETY: Changes in Renal Function (Blood Urea Nitrogen) After Treatment up to 90 Days After Randomization(Within 90 days of randomization)
  • SAFETY: Changes in Renal Function (Estimated Glomerular Filtration Rate) After Treatment up to 90 Days After Randomization(Within 90 days of randomization)
  • EFFICACY: Total Weight Loss During the Index Hospitalization(Index Hospitalization, an average of 8 days)
  • EFFICACY: Time to Freedom From Congestion(Index Hospitalization, an average of 8 days)
  • EFFICACY: Freedom From Congestion(Index Hospitalization, an average of 8 days)
  • CLINICAL: Total Number of Days Rehospitalized for Heart Failure (HF) at 30 and 90 Days After Discharge(Within 30 days and 90 days after hospital discharge)
  • CLINICAL: Total Number of Heart Failure (HF) Rehospitalizations at 30 and 90 Days After Discharge(Within 30 days and 90 days after hospital discharge)
  • CLINICAL: All Cause Rehospitalization Rates at 30 and 90 Days(Within 30 days and 90 days after hospital discharge)
  • Days Alive and Out of Hospital at 30 and 90 Days After Discharge(Within 30 and 90 days after hospital discharge)
  • CLINICAL: Total Number of Days for Cardiovascular (CV) Rehospitalizations at 30 and 90 Days After Discharge(Within 30 days and 90 days after hospital discharge)
  • Mortality Rates Within Index Hospitalization or Within 90 Days After Hospital Discharge.(Time from randomization to 90 days post-hospital discharge)
  • SAFETY: Changes in Renal Function (Blood Urea Nitrogen/Serum Creatinine) After Treatment up to 90 Days After Randomization(Within 90 days of randomization)
  • CLINICAL: Global Clinical Score at 30 and 90 Days After Discharge(Within 90 days after hospital discharge)

Study Sites (38)

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