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High Cut-Off Continuous Veno-venous Hemodialysis (CVVHD) in Patients Treated for Acute Renal Failure After Systemic Inflammatory Response Syndrome (SIRS)/Septic Shock (HICOSS)

Primary Purpose

Systemic Inflammatory Response Syndrome, Kidney Failure, Acute

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
continuous venovenous hemodialysis
Sponsored by
Baxter Healthcare Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Systemic Inflammatory Response Syndrome

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Fulfilling at least two of the SIRS criteria as defined by the American College of Chest Physicians (ACCP)/Society of Critical Care Medicine (SCCM) Consensus Conference
  2. Having signs of renal dysfunction
  3. Requirement for catecholamine administration (norepinephrine or others)
  4. Acute Physiology And Chronic Health Evaluation (APACHE II) score at enrolment greater than or equal to 19 and less than or equal to 30

Exclusion Criteria:

  1. Lack of written informed consent from patients or a legally authorized surrogate
  2. Duration of septic shock greater than 4 days
  3. Hypoproteinemia (characterized by serum albumin less than 18 g/l)
  4. End stage renal failure
  5. Known active malignancy
  6. Known human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV) infection
  7. Age younger than 18 years or older than 80 years
  8. Known pregnancy
  9. Immunosuppression after transplantation
  10. Participation in another clinical study
  11. Renal replacement therapy greater than 24 hours before randomization

Sites / Locations

  • Leopold Franzens Universität Innsbruck
  • Medizinische Klinik mit Schwerpunkt Nephrologie Charite, Campus Mitte
  • Charité-Virchow Klinik
  • Universitätsklinikum Tübingen

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

HCO

control

Arm Description

High cut-off filters HCO1100

conventional high-flux filters

Outcomes

Primary Outcome Measures

Dosage of vasopressors
Mean arterial pressure
Heart rate
Central venous pressure

Secondary Outcome Measures

Sequential organ failure assessment (SOFA) score
Survival
Length of need for catecholamine application
Length of need for mechanical ventilation
Length of need for renal replacement therapy
Length of stay in intensive care unit (ICU)

Full Information

First Posted
January 9, 2009
Last Updated
March 5, 2018
Sponsor
Baxter Healthcare Corporation
Collaborators
Gambro Dialysatoren GmbH
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1. Study Identification

Unique Protocol Identification Number
NCT00875888
Brief Title
High Cut-Off Continuous Veno-venous Hemodialysis (CVVHD) in Patients Treated for Acute Renal Failure After Systemic Inflammatory Response Syndrome (SIRS)/Septic Shock
Acronym
HICOSS
Official Title
High Cut-off Continuous Venovenous Hemodialysis (CVVHD) to Improve Hemodynamic Stability and Organ Function Scores in Patients Treated for Acute Renal Failure After Systemic Inflammatory Response Syndrome (SIRS)/Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Terminated
Why Stopped
based on interim analysis statistical significance in primary endpoint cannot be achieved with planned sample size, no safety concerns
Study Start Date
February 2004 (undefined)
Primary Completion Date
June 2009 (Actual)
Study Completion Date
June 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Baxter Healthcare Corporation
Collaborators
Gambro Dialysatoren GmbH

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will assess the influence of the High Cut-Off (HCO) CVVHD treatment on the disease progression in septic patients. The primary aim of the study is to evaluate whether HCO CVVHD leads to a significant improvement of the hemodynamic status (mean arterial pressure, vasopressor requirements) in septic patients in comparison to CVVHD treatment with conventional high-flux filters. For the HCO-group the investigators expect a 50% lower dosage of vasopressors needed to maintain an adequate organ perfusion.
Detailed Description
Severe sepsis is a devastating disorder that results from a complex host response to insult after infection. Despite advances in intensive care technologies sepsis remains an important and life-threatening problem. Sepsis is the most common cause of death in the intensive care unit. Local or systemic release of bacteria-derived compounds, leading to the production of proinflammatory cytokines, induce systemic inflammatory reactions in septic patients. Continuous renal replacement therapies (CRRT) such as hemodialysis (CVVHD), hemofiltration (CVVH) or hemodiafiltration (CVVHDF) with conventional high-flux membranes allow to control fluid and electrolyte balance, and to improve the hemodynamic status of the patients. However, conventional high flux membranes have a limited permeability for sepsis-associated mediators with molecular weights in the range of 15.000 to 60.000 Da. A promising approach to enhance the mediator removal is to use membranes having larger pores and permeability characteristics than those currently used in CRRT. For that purpose a High Cut-Off (HCO) membrane has been developed and is manufactured by Gambro Research.After demonstrating the safety as well as the cytokine removal effectiveness in a clinical pilot study this study will assess the influence of the HCO treatment on the disease progression in septic patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Inflammatory Response Syndrome, Kidney Failure, Acute

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HCO
Arm Type
Experimental
Arm Description
High cut-off filters HCO1100
Arm Title
control
Arm Type
Active Comparator
Arm Description
conventional high-flux filters
Intervention Type
Device
Intervention Name(s)
continuous venovenous hemodialysis
Intervention Description
dialysate flow rate 35 ml/h/kg. Blood flow rate should be aimed at 200 ml/min, but not less than 150 ml/min. Bicarbonate- or lactate-buffered solutions will be used as dialysis fluids. Study dialyzers will be changed routinely every 24 h or earlier if the filter is obstructed by clotting.
Primary Outcome Measure Information:
Title
Dosage of vasopressors
Time Frame
day 1 to day 5
Title
Mean arterial pressure
Time Frame
day before inclusion and day 1 to day 5
Title
Heart rate
Time Frame
day before inclusion and day 1 to day 5
Title
Central venous pressure
Time Frame
day before inclusion and day 1 to day 5
Secondary Outcome Measure Information:
Title
Sequential organ failure assessment (SOFA) score
Time Frame
at ICU admission, at inclusion and day 1 to day 5
Title
Survival
Time Frame
28 days
Title
Length of need for catecholamine application
Time Frame
28 days follow up
Title
Length of need for mechanical ventilation
Time Frame
28 days
Title
Length of need for renal replacement therapy
Time Frame
28 days
Title
Length of stay in intensive care unit (ICU)
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Fulfilling at least two of the SIRS criteria as defined by the American College of Chest Physicians (ACCP)/Society of Critical Care Medicine (SCCM) Consensus Conference Having signs of renal dysfunction Requirement for catecholamine administration (norepinephrine or others) Acute Physiology And Chronic Health Evaluation (APACHE II) score at enrolment greater than or equal to 19 and less than or equal to 30 Exclusion Criteria: Lack of written informed consent from patients or a legally authorized surrogate Duration of septic shock greater than 4 days Hypoproteinemia (characterized by serum albumin less than 18 g/l) End stage renal failure Known active malignancy Known human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV) infection Age younger than 18 years or older than 80 years Known pregnancy Immunosuppression after transplantation Participation in another clinical study Renal replacement therapy greater than 24 hours before randomization
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Werner Beck, Dr.
Organizational Affiliation
Gambro Dialysatoren GmbH
Official's Role
Study Director
Facility Information:
Facility Name
Leopold Franzens Universität Innsbruck
City
Innsbruck
ZIP/Postal Code
6020
Country
Austria
Facility Name
Medizinische Klinik mit Schwerpunkt Nephrologie Charite, Campus Mitte
City
Berlin
ZIP/Postal Code
10117
Country
Germany
Facility Name
Charité-Virchow Klinik
City
Berlin
ZIP/Postal Code
13353
Country
Germany
Facility Name
Universitätsklinikum Tübingen
City
Tübingen
ZIP/Postal Code
72076
Country
Germany

12. IPD Sharing Statement

Citations:
PubMed Identifier
16763508
Citation
Morgera S, Haase M, Kuss T, Vargas-Hein O, Zuckermann-Becker H, Melzer C, Krieg H, Wegner B, Bellomo R, Neumayer HH. Pilot study on the effects of high cutoff hemofiltration on the need for norepinephrine in septic patients with acute renal failure. Crit Care Med. 2006 Aug;34(8):2099-104. doi: 10.1097/01.CCM.0000229147.50592.F9.
Results Reference
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PubMed Identifier
14605279
Citation
Morgera S, Haase M, Rocktaschel J, Bohler T, von Heymann C, Vargas-Hein O, Krausch D, Zuckermann-Becker H, Muller JM, Kox WJ, Neumayer HH. High permeability haemofiltration improves peripheral blood mononuclear cell proliferation in septic patients with acute renal failure. Nephrol Dial Transplant. 2003 Dec;18(12):2570-6. doi: 10.1093/ndt/gfg435.
Results Reference
background
PubMed Identifier
12955174
Citation
Morgera S, Rocktaschel J, Haase M, Lehmann C, von Heymann C, Ziemer S, Priem F, Hocher B, Gohl H, Kox WJ, Buder HW, Neumayer HH. Intermittent high permeability hemofiltration in septic patients with acute renal failure. Intensive Care Med. 2003 Nov;29(11):1989-95. doi: 10.1007/s00134-003-2003-9. Epub 2003 Sep 3.
Results Reference
background
PubMed Identifier
12902634
Citation
Morgera S, Haase M, Rocktaschel J, Bohler T, Vargas-Hein O, Melzer C, Krausch D, Kox WJ, Baumann G, Beck W, Gohl H, Neumayer HH. Intermittent high-permeability hemofiltration modulates inflammatory response in septic patients with multiorgan failure. Nephron Clin Pract. 2003;94(3):c75-80. doi: 10.1159/000072024.
Results Reference
background
PubMed Identifier
14981602
Citation
Morgera S, Slowinski T, Melzer C, Sobottke V, Vargas-Hein O, Volk T, Zuckermann-Becker H, Wegner B, Muller JM, Baumann G, Kox WJ, Bellomo R, Neumayer HH. Renal replacement therapy with high-cutoff hemofilters: Impact of convection and diffusion on cytokine clearances and protein status. Am J Kidney Dis. 2004 Mar;43(3):444-53. doi: 10.1053/j.ajkd.2003.11.006.
Results Reference
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High Cut-Off Continuous Veno-venous Hemodialysis (CVVHD) in Patients Treated for Acute Renal Failure After Systemic Inflammatory Response Syndrome (SIRS)/Septic Shock

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