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Completed

NCT Number: NCT00608491

Effectiveness of Ultrafiltration in Treating People With Acute Decompensated Heart Failure and Cardiorenal Syndrome (The CARRESS Study)

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Montreal Heart Institute, Montreal, Quebec, Canada

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 18 or older
  • admitted to the hospital with a primary diagnosis of decompensated heart failure
  • onset of cardiorenal syndrome after hospitalization or pre-hospitalization
  • after hospitalization - onset of cardiorenal syndrome after hospitalization must occur within 10 days from the time of admission after receiving IV diuretics
  • pre-hospitalization - onset of cardiorenal syndrome pre-hospitalization must occur within 12 weeks of the index hospitalization in the setting of escalating doses of outpatient diuretics
  • persistent volume overload

Exclusion criteria

  • intravascular volume depletion based on investigator"s clinical assessment
  • acute coronary syndrome within 4 weeks
  • indication for hemodialysis
  • creatinine > 3.5 mg per deciliter at admission to the hospital
  • systolic blood pressure < 90 mmHg at the time of enrollment
  • alternative explanation for worsening renal function such as obstructive nephropathy,contrast induced nephropathy, acute tubular necrosis
  • Hematocrit > 45%
  • poor venous access
  • clinical instability likely to require the addition of intravenous vasoactive drugs including vasodilators and/or inotropic agents
  • allergy or contraindications to the use of heparin
  • the use of iodinated radio contrast material in the last 72 hours or anticipated use of IV contrast during the current hospitalization
  • known bilateral renal artery stenosis
  • active myocarditis
  • hypertrophic obstructive cardiomyopathy
  • severe valvular stenosis
  • complex congenital heart disease
  • sepsis or ongoing systemic infection
  • enrollment in another clinical trial involving medical or device based interventions

Treatment and study plan

Stepped pharmacologic care

Drug

Stepped care will provide treating physicians with guidelines for the intensification of diuretic therapy and the possible use of vasodilators and inotropes.

Ultrafiltration

Device

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.

Primary outcomes

  1. Change in Serum Creatinine

    Time frame: Change from Baseline to Day 4

  2. Change in Weight

    Time frame: Change from Baseline to Day 4

Secondary outcomes

  1. Change in Glomerular Filtration Rate

    Time frame: Change from Baseline to Day 4

  2. Change in Serum Creatinine

    Time frame: Change from Baseline to Day 7

  3. Change in Glomerular Filtration Rate

    Time frame: Change from Baseline to Day 7

  4. Changes in Weight

    Time frame: Change from Baseline to Day 1

  5. Changes in Weight

    Time frame: Change from Baseline to Day 2

  6. Change in Weight

    Time frame: Change from Baseline to Day 3

  7. Changes in Weight

    Time frame: Change from Baseline to Day 5

  8. Change in Weight

    Time frame: Change from Baseline to Day 6

  9. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 1

  10. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 2

  11. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 3

  12. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 4

  13. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 5

  14. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 6

  15. Cumulative Net Fluid Loss

    Time frame: Randomization through Day 7

  16. Dyspnea Visual Analog Scale

    Time frame: Change from Baseline to Day 4

    Scale range: -100 , +100

    -100=worse, +100=better

  17. Change in Global Visual Analog Scale

    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".

  18. Change in Dyspnea Visual Analog Scale

    Time frame: Baseline to Day 7/Discharge

    Scale range: -100 , +100

    -100=worse, +100=better

  19. Change in Global Visual Analog Scale

    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".

  20. Change in Furosemide-Equivalent Dose

    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)

  21. Change in Blood Sodium Level

    Time frame: Baseline to Day 4

  22. Change in Blood Potassium Level

    Time frame: Baseline to Day 4

  23. Change in Blood Urea Nitrogen/Urea

    Time frame: Baseline to Day 4

  24. Change in Blood Bicarbonate Level

    Time frame: Baseline to Day 4

  25. Change in Blood Hemoglobin Level

    Time frame: Baseline to Day 4

  26. Change in Blood Sodium Level

    Time frame: Baseline to Day 7/Discharge

  27. Change in Blood Potassium Level

    Time frame: Baseline to Day 7/Discharge

  28. Change in Blood Urea Nitrogen/Urea

    Time frame: Baseline to Day 7/Discharge

  29. Change in Blood Bicarbonate Level

    Time frame: Baseline to Day 7/Discharge

  30. Change in Blood Hemoglobin Level

    Time frame: Baseline to Day 7/Discharge

  31. Change in Blood Cystatin C

    Time frame: Baseline to Day 4

  32. Change in Uric Acid

    Time frame: Baseline to Day 4

  33. Change in Blood N- Terminal Pro- BNP

    Time frame: Baseline to Day 4

  34. Change in Plasma Renin Activity

    Time frame: Baseline to Day 4

  35. Change in Blood High Sensitivity Troponin I

    Time frame: Baseline to Day 4

  36. Change in Blood Aldosterone

    Time frame: Baseline to Day 4

  37. Change in Blood Procollagen III N-terminal Propepide

    Time frame: Baseline to Day 4

  38. Change in Blood Endothelin-1

    Time frame: Baseline to Day 4

  39. Change in Blood High Sensitivity C-Reactive Protein

    Time frame: Baseline to Day 4

  40. Change in Blood Carboxy-terminal Telopeptide of Collagen Type I

    Time frame: Baseline to Day 4

  41. Change in Blood Cystatin C

    Time frame: Baseline to Day 7/Discharge

  42. Change in Blood Uric Acid

    Time frame: Baseline to Day 7/Discharge

  43. Change in Blood N Terminal Pro-Natriuretic Peptide

    Time frame: Baseline to Day 7/Discharge

  44. Change in Plasma Renin Activity

    Time frame: Baseline to Day 7/Discharge

  45. Change in Blood High Sensitivity Troponin I

    Time frame: Baseline to Day 7/Discharge

  46. Change in Blood Aldosterone

    Time frame: Baseline to Day 7/Discharge

  47. Change in Blood Procollagen III N-terminal Propepide

    Time frame: Baseline to Day 7/Discharge

  48. Change in Blood Endothelin-1

    Time frame: Baseline to Day 7/Discharge

  49. Change in Blood Carboxy-terminal Telopeptide of Collagen Type I

    Time frame: Baseline to Day 7/Discharge

  50. Change in Blood High Sensitivity C-Reactive Protein

    Time frame: Baseline to Day 7/Discharge

  51. Weight Change

    Time frame: Baseline to Day 30

  52. Change in Furosemide-Equivalent Dose

    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)

  53. Creatinine Change

    Time frame: Baseline to Day 30

  54. Glomerular Filtration Rate Change

    Time frame: Baseline to Day 30

  55. Weight Change

    Time frame: Baseline to Day 60

  56. Change in Furosemide-Equivalent Dose

    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)

  57. Best Available Serum Creatinine Change

    Time frame: Baseline to Day 60

    Core laboratory when available. If not available, local laboratory results were used.

  58. Best Available Glomerular Filtration Rate Change

    Time frame: Baseline to Day 60

    Core laboratory when available. If not available, local laboratory results were used.

  59. Change in Blood Uric Acid

    Time frame: Baseline to Day 60

  60. Change in Blood Cystatin C

    Time frame: Baseline to Day 60

  61. Change in Blood N Terminal Pro - B Natriuretic Peptides

    Time frame: Baseline to Day 60

  62. Change in Plasma Renin Activity

    Time frame: Baseline to Day 60

  63. Change in Blood High Sensitivity Troponin I

    Time frame: Baseline to Day 60

  64. Change in Blood Aldosterone

    Time frame: Baseline to Day 60

  65. Change in Blood Procollagen III N-terminal Propepide

    Time frame: Baseline to Day 60

  66. Change in Blood Endothelin-1

    Time frame: Baseline to Day 60

  67. Change in Blood High Sensitivity C-Reactive Protein

    Time frame: Baseline to Day 60

  68. Change in Blood Carboxy-terminal Telopeptide of Collagen Type I

    Time frame: Baseline to Day 60

Sponsors and collaborators

Lead sponsor

Duke University

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • Nuwellis, Inc.

Registry information

Official study title

CARdiorenal REScue Study in Acute Decompensated Heart Failure: CARRESS

Acronym: CARRESS

Important dates

Study start
2008
Primary completion
2012
Study completion
2012
First posted
Feb 6, 2008
Registry last updated
Jun 24, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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