Stepped pharmacologic care
DrugStepped care will provide treating physicians with guidelines for the intensification of diuretic therapy and the possible use of vasodilators and inotropes.
NCT Number: NCT00608491
Heart failure is a serious condition in which the heart's ability to pump blood through the body is impaired, often making a person feel weak or fatigued. When a person's condition worsens to the point of hospitalization, that person is said to have acute decompensated heart failure (ADHF). Abnormal kidney function in association with cardiac distress, known as cardiorenal syndrome, is a common complication of heart failure and causes further medical problems and need for hospitalization. While there are various effective treatments for heart failure, more research is needed to determine the best treatment for targeting both ADHF and cardiorenal syndrome. This study will compare the safety and effectiveness of ultrafiltration versus standard medical drug therapy in improving renal function and relieving fluid buildup in people hospitalized with ADHF and cardiorenal syndrome.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Montreal Heart Institute, Montreal, Quebec, Canada
Heart failure is a common condition that affects approximately 5 million people in the United States, with 550,000 new cases diagnosed each year. Common symptoms of heart failure include swelling and fluid buildup in the legs, feet, and/or lungs; shortness of breath; coughing; elevated heart rate; change in appetite; and fatigue. If left untreated, the condition of the heart may deteriorate so far that the person undergoes ADHF. The number of hospitalizations attributed to ADHF has risen significantly, with many people readmitted soon after discharge because of recurring symptoms or further medical complications, such as cardiorenal syndrome. Current heart failure treatments focus on removing excess fluid buildup, often by increasing urination with diuretic medications or by draining directly from the veins. Direct drainage from the veins, also known as ultrafiltration, may be the more effective method for treating people with ADHF and cardiorenal syndrome. This study will compare the safety and effectiveness of ultrafiltration versus standard medical drug therapy in improving renal function and relieving fluid buildup in people hospitalized with ADHF and cardiorenal syndrome.
Participation in this study will last 60 days. All potential participants will undergo initial screening, which will include a medical history, physical exam, blood draws, measurements of fluid intake and urine output, and questionnaires. These same evaluations and procedures will be repeated at various points during the hospital stay. Eligible participants will be randomly assigned to receive standard medical drug therapy or fluid removal by ultrafiltration. Standard medical drug therapy will involve the intravenous delivery of diuretics and possibly other doctor-recommended medications. Ultrafiltration will involve intravenously removing blood, passing it through an ultrafiltration device, and then returning the blood to the participant. During ultrafiltration, participants will be treated with a blood thinner through the IV, as well.
Follow-up assessments will occur at Days 30 and 60 after treatment. Follow-up assessments will include measurements of fluid intake, urine output, and vital signs; blood draws; physical exams; and questions about medications and status of recovery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Stepped care will provide treating physicians with guidelines for the intensification of diuretic therapy and the possible use of vasodilators and inotropes.
All loop diuretics will be discontinued. Treatment will involve slow continuous ultrafiltration until an optimal volume status has been achieved. Ultrafiltration therapy will be initiated after the placement of appropriate intravenous access and will continue until the participant's signs and symptoms of congestion have been optimized. Fluid status will be managed exclusively by ultrafiltration using the Aquadex system 100 (CHF Solutions, Inc.) according to the manufacturer's specifications. The use of vasodilators or inotropic agents will be prohibited unless deemed necessary for rescue therapy.
Time frame: Change from Baseline to Day 4
Time frame: Change from Baseline to Day 4
Time frame: Change from Baseline to Day 4
Time frame: Change from Baseline to Day 7
Time frame: Change from Baseline to Day 7
Time frame: Change from Baseline to Day 1
Time frame: Change from Baseline to Day 2
Time frame: Change from Baseline to Day 3
Time frame: Change from Baseline to Day 5
Time frame: Change from Baseline to Day 6
Time frame: Randomization through Day 1
Time frame: Randomization through Day 2
Time frame: Randomization through Day 3
Time frame: Randomization through Day 4
Time frame: Randomization through Day 5
Time frame: Randomization through Day 6
Time frame: Randomization through Day 7
Time frame: Change from Baseline to Day 4
Scale range: -100 , +100
-100=worse, +100=better
Time frame: Change from Baseline to Day 4
Scale range: -100 , +100
-100=worse, +100=better Participants asked to mark their global well being on a 10 cm vertical line, with the top labeled "best you have ever felt" and the bottom labeled "worst you have ever felt".
Time frame: Baseline to Day 7/Discharge
Scale range: -100 , +100
-100=worse, +100=better
Time frame: Baseline to Day 7/Discharge
Scale range: -100 , +100
-100=worse, +100=better Participants asked to mark their global well being on a 10 cm vertical line, with the top labeled "best you have ever felt" and the bottom labeled "worst you have ever felt".
Time frame: Baseline to Day 7/Discharge
Furosemide-Equivalent Dose is the dose bumetanide or torsemide converted to furosemide equivalent (Torsemide dose x 2,Bumetanide dose x 40)
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 4
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 7/Discharge
Time frame: Baseline to Day 30
Time frame: Baseline to Day 30
Furosemide-Equivalent Dose is the dose bumetanide or torsemide converted to furosemide equivalent (Torsemide dose x 2,Bumetanide dose x 40)
Time frame: Baseline to Day 30
Time frame: Baseline to Day 30
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Furosemide-Equivalent Dose is the dose bumetanide or torsemide converted to furosemide equivalent (Torsemide dose x 2,Bumetanide dose x 40)
Time frame: Baseline to Day 60
Core laboratory when available. If not available, local laboratory results were used.
Time frame: Baseline to Day 60
Core laboratory when available. If not available, local laboratory results were used.
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Time frame: Baseline to Day 60
Duke University
Other
CARdiorenal REScue Study in Acute Decompensated Heart Failure: CARRESS
Acronym: CARRESS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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