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Ultrafiltration Versus Intravenous (IV) Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: (UNLOAD)

Primary Purpose

Congestive Heart Failure

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Aquadex system
IV diuretic
Sponsored by
Nuwellis, Inc.
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congestive Heart Failure focused on measuring Ultrafiltration, acute decompensated heart failure, fluid overload, pulmonary congestion

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patients hospitalized with primary diagnosis of acute decompensated congestive heart failure (adCHF) Evidence of fluid overload as indicated by: pitting edema (2+) of lower extremities; jugular venous distension; pulmonary edema or pleural effusion; ascites; paroxysmal nocturnal dyspnea or 2-pillow orthopnea Exclusion Criteria: Acute coronary syndrome Creatinine greater than 3.0 Systolic blood pressure less than or equal to 90 mmHg Hematocrit greater than 45% Prior administration of IV vasoactive drugs in the emergency room (ER) Clinical instability requiring pressors during hospitalization Recent use of iodinated contrast material Severe concomitant disease expected to prolong hospitalization Sepsis On or requires renal dialysis Had a cardiac transplant Heparin allergy

Sites / Locations

  • Midwest Heart Institute

Outcomes

Primary Outcome Measures

Total weight loss during first 48 hours of randomization
Change in dyspnea score during first 48 hours of randomization

Secondary Outcome Measures

Change in global assessment
Change in quality of life (living with heart failure)
Changes in brain natriuretic peptide (BNP)
Changes in 6 minute walk test
Total fluid loss during first 48 hours of randomization
Changes in blood urea nitrogen (BUN) and creatinine
Changes in renin and aldosterone

Full Information

First Posted
July 25, 2005
Last Updated
March 14, 2007
Sponsor
Nuwellis, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT00124137
Brief Title
Ultrafiltration Versus Intravenous (IV) Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: (UNLOAD)
Official Title
Ultrafiltration Versus IV Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: A Prospective Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2005
Overall Recruitment Status
Completed
Study Start Date
April 2004 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
October 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Nuwellis, Inc.

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to compare patients who are suffering from heart failure and who are fluid overloaded to determine if ultrafiltration (UF) can remove more of the extra fluid as measured by weight loss while in the hospital and improve the patient's breathing.
Detailed Description
Congestive heart failure is an important public health issue. It remains the leading cause of hospitalization in Medicare beneficiaries. Ninety percent of all hospitalizations for CHF are due to fluid overload. Most of the expense related to the management of heart failure is due to hospital-based care; interventions that reduce the amount of time patients spend in the hospital may greatly decrease the cost associated with caring for these patients. Hospital stay for patients admitted for acute decompensated congestive heart failure (adCHF) is largely dictated by how quickly the signs and symptoms of congestion can be relieved and whether ACE inhibitors can be started safely. Diuretics are usually effective in relieving congestion, but achieving adequate diuresis often requires a process of trial and error. Some patients are simply refractory to oral or intravenous diuretics. Diuretics stimulate adverse neurohormonal systems and can cause progressive azotemia. Bayliss (1977) showed that there is a significant increase in renin and aldosterone levels as a response to diuretic treatment rather than as a result of the heart failure itself. Gottlieb (2002) showed that loop diuretics diminish glomerular filtration rate in patients with heart failure. In addition, as more diuretics are given, serum electrolyte imbalances often occur, requiring additional monitoring of patients. UF has been used as a therapeutic method to remove excessive fluid in patients for over 30 years. UF removes excess water without causing a significant clinical change in the electrolyte composition of the blood or causes adverse affects on the kidneys and neurohormonal system. Studies have shown that UF increases urine output, increases responsiveness to standard oral therapies and decreases readmission rate. While the usefulness of UF in this patient population has great potential, this form of therapy is not usually performed due to the need for invasive venous access and increased expense i.e. high flow dialysis machines. CHF Solutions has developed the Aquadex System that has FDA market clearance for UF. The advantage of the Aquadex System is its simplicity and the fact that it can be administered by means of peripheral catheters or with a central venous access. Early prospective series and subsequent clinical experience involving adCHF patients have shown that 4 to 8 liters can easily be withdrawn in a short amount of time using the peripheral access approach with the Aquadex System. Volume removal was not associated with disruption of electrolyte balance, worsening of renal distress or impact on blood pressure or heart rate of clinical significance. The Aquadex System is a predictable, safe, and effective way to ensure adequate volume removal that may result in shorter hospital stays, better symptom relief and more efficient dosing of medications for the treatment of adCHF. The purpose of this study is to determine whether the Aquadex System can improve the acute management of patients with adCHF and maintain this improvement over a period of time compared to IV diuretics. Ultrafiltration in this patient population may decrease length of hospital stay and reduce hospital readmissions for heart failure leading to a significant reduction in costs for the treatment of these patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congestive Heart Failure
Keywords
Ultrafiltration, acute decompensated heart failure, fluid overload, pulmonary congestion

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
Aquadex system
Intervention Type
Drug
Intervention Name(s)
IV diuretic
Primary Outcome Measure Information:
Title
Total weight loss during first 48 hours of randomization
Title
Change in dyspnea score during first 48 hours of randomization
Secondary Outcome Measure Information:
Title
Change in global assessment
Title
Change in quality of life (living with heart failure)
Title
Changes in brain natriuretic peptide (BNP)
Title
Changes in 6 minute walk test
Title
Total fluid loss during first 48 hours of randomization
Title
Changes in blood urea nitrogen (BUN) and creatinine
Title
Changes in renin and aldosterone

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients hospitalized with primary diagnosis of acute decompensated congestive heart failure (adCHF) Evidence of fluid overload as indicated by: pitting edema (2+) of lower extremities; jugular venous distension; pulmonary edema or pleural effusion; ascites; paroxysmal nocturnal dyspnea or 2-pillow orthopnea Exclusion Criteria: Acute coronary syndrome Creatinine greater than 3.0 Systolic blood pressure less than or equal to 90 mmHg Hematocrit greater than 45% Prior administration of IV vasoactive drugs in the emergency room (ER) Clinical instability requiring pressors during hospitalization Recent use of iodinated contrast material Severe concomitant disease expected to prolong hospitalization Sepsis On or requires renal dialysis Had a cardiac transplant Heparin allergy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria R Costanzo, MD
Organizational Affiliation
Midwest Heart
Official's Role
Principal Investigator
Facility Information:
Facility Name
Midwest Heart Institute
City
Lombard
State/Province
Illinois
ZIP/Postal Code
60148
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17291932
Citation
Costanzo MR, Guglin ME, Saltzberg MT, Jessup ML, Bart BA, Teerlink JR, Jaski BE, Fang JC, Feller ED, Haas GJ, Anderson AS, Schollmeyer MP, Sobotka PA; UNLOAD Trial Investigators. Ultrafiltration versus intravenous diuretics for patients hospitalized for acute decompensated heart failure. J Am Coll Cardiol. 2007 Feb 13;49(6):675-83. doi: 10.1016/j.jacc.2006.07.073. Epub 2007 Jan 26. Erratum In: J Am Coll Cardiol. 2007 Mar 13;49(10):1136.
Results Reference
derived

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Ultrafiltration Versus Intravenous (IV) Diuretics for Patients Hospitalized for Acute Decompensated Heart Failure: (UNLOAD)

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