Adjuvant Therapy With CytoSorb in Refractory Septic Shock (ACYSS)
Primary Purpose
Septic Shock
Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
CytoSorb-Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Septic Shock focused on measuring Sepsis, Critically ill, Intensive care medicine, CytoSorb, Hemoadsorption, Pharmacokinetic
Eligibility Criteria
Inclusion Criteria:
- Refractory septic shock
- Need for Norepinephrine ≥ 0.25 µg/kg/min
- IL6 ≥ 1000 ng/l
- Indication for CRRT
Exclusion Criteria:
- Sepsis due to pulmonary or urogenital causes
- Onset of septic shock longer than 36 hours
- Liver cirrhosis Child Pugh C
- "do not resuscitate"-order
- expected survival < 14 days
- participation in another interventional trial
- Pregnancy or breastfeeding
- Lack of consent
Sites / Locations
- University Medical Center Hamburg-EppendorfRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
CytoSorb-Therapy
Standard of care
Arm Description
Therapy of septic shock using guideline directed standard of care, including continuous renal replacement therapy in combination with haemadsorption using CytoSorb-Adsorber
Therapy of septic shock using guideline directed standard of care, including continuous renal replacement therapy
Outcomes
Primary Outcome Measures
Percentage of patients with a reduction of catecholamine dose of at least 25% within the first 48 hours of treatment
Percentage of patients with a reduction of catecholamine dose of at least 25% compared to baseline for at least 6 hours within the first 48 hours of treatment.
Secondary Outcome Measures
Change in organ dysfunction
Change in organ dysfunction based on "Sequential Organ Failure Assessment" (SOFA) Score The SOFA score is made of 6 variables, each representing an organ system. Each organ system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure) The worst physiological variables were collected serially every 24 hours of a patient's ICU admission. The "worst" measurement was defined as the measure that correlated to the highest number of points. The SOFA score ranges from 0 to 24.
Lactate clearance
Improving lactate clearance by lowering serum lactate levels
Renal replacement therapy
Time with need for renal replacement therapy
Percentage of patients with a reduction of catecholamine dose of at least 25% within the first 24 hours of treatment
Percentage of patients with a reduction of catecholamine dose of at least 25% compared to baseline for at least 6 hours within the first 48 hours of treatment.
End of septic shock
Time until shock resolution
ICU length of stay
ICU length of stay
Time on mechanical ventilation
Time on mechanical ventilation
Cumulative catecholamine dose
Cumulative catecholamine dose
Overall and ICU mortality
Overall and ICU mortality
Serum levels of administered anti-infectives
Serum drug Levels of pre and post filter and adsorber system on day 1-3 while CytoSorb therapy (sampling: t 0, 1, 2, 6, 8, 12, 24 h after CytoSorb initiation)
Change of plasma Interleukin-6 (IL6) level
Change of plasma Interleukin-6 (IL6) level
Change of plasma Interleukin-10 (IL10) level
Change of plasma Interleukin-10 (IL10) level
Change of plasma Procalcitonin (PCT) level
Change of plasma Procalcitonin (PCT) level
Change of HLA-DR level
Change of HLA-DR (Human Leukocyte Antigen - DR isotype) level of monocytes
Change of TNF alpha level after ex-vivo stimulation
Change of TNF-alfa level (Tumor Necrosis Factor alpha) level after LPS (Lipopolysaccharides) stimulation as sign of monocytic immunocompetence
Full Information
NCT ID
NCT04013269
First Posted
June 15, 2019
Last Updated
November 6, 2022
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
CytoSorbents, Inc
1. Study Identification
Unique Protocol Identification Number
NCT04013269
Brief Title
Adjuvant Therapy With CytoSorb in Refractory Septic Shock
Acronym
ACYSS
Official Title
Effect of the CytoSorb Adsorber on Hemodynamic, Immunological and Pharmacokinetic Parameters in Refractory Septic Shock
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2020 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
CytoSorbents, Inc
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 prospective randomized single center study investigates to what extent the removal of elevated cytokine levels by hemoadsorption has a positive effect on the treatment of patients in septic shock by stabilizing the circulatory situation.
Detailed Description
The term "sepsis" refers to a clinical syndrome in which a dysregulation of the host's inflammatory reaction to infection leads to a life-threatening of organ dysfunctions. Sepsis and septic shock are major causes of death in intensive care units worldwide.
The clinical picture of septic shock, the most severe form of sepsis, leads to uncontrolled production and release of a large number of proinflammatory cytokines and mediators, the "cytokine storm". Septic shock is accompanied by a massive increase in mortality of up to 60%.
This high mortality rate is due to a lack of current treatment options. The early recognition of the disease and its immediate treatment are decisive for successful therapy and the survival of those affected. The most important therapeutic steps, apart from focus control by antibiotics and surgical intervention, are the stabilization of the affected organ systems, in particular the circulatory system and the respiratory system. As an extracorporeal and non-specific procedure for the interruption of the cytokine storm, hemoadsorption by means of CytoSorb adsorbers may be an intervention, which has already demonstrated its basic effectiveness in the treatment of septic and cardiosurgical patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Septic Shock
Keywords
Sepsis, Critically ill, Intensive care medicine, CytoSorb, Hemoadsorption, Pharmacokinetic
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CytoSorb-Therapy
Arm Type
Active Comparator
Arm Description
Therapy of septic shock using guideline directed standard of care, including continuous renal replacement therapy in combination with haemadsorption using CytoSorb-Adsorber
Arm Title
Standard of care
Arm Type
No Intervention
Arm Description
Therapy of septic shock using guideline directed standard of care, including continuous renal replacement therapy
Intervention Type
Device
Intervention Name(s)
CytoSorb-Therapy
Intervention Description
Additional use of Cytosorb-Adsorber in patients with septic shock and need for continuous renal replacement therapy
Primary Outcome Measure Information:
Title
Percentage of patients with a reduction of catecholamine dose of at least 25% within the first 48 hours of treatment
Description
Percentage of patients with a reduction of catecholamine dose of at least 25% compared to baseline for at least 6 hours within the first 48 hours of treatment.
Time Frame
48 hours
Secondary Outcome Measure Information:
Title
Change in organ dysfunction
Description
Change in organ dysfunction based on "Sequential Organ Failure Assessment" (SOFA) Score The SOFA score is made of 6 variables, each representing an organ system. Each organ system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure) The worst physiological variables were collected serially every 24 hours of a patient's ICU admission. The "worst" measurement was defined as the measure that correlated to the highest number of points. The SOFA score ranges from 0 to 24.
Time Frame
10 days
Title
Lactate clearance
Description
Improving lactate clearance by lowering serum lactate levels
Time Frame
10 days
Title
Renal replacement therapy
Description
Time with need for renal replacement therapy
Time Frame
10 days
Title
Percentage of patients with a reduction of catecholamine dose of at least 25% within the first 24 hours of treatment
Description
Percentage of patients with a reduction of catecholamine dose of at least 25% compared to baseline for at least 6 hours within the first 48 hours of treatment.
Time Frame
24 hours
Title
End of septic shock
Description
Time until shock resolution
Time Frame
10 days
Title
ICU length of stay
Description
ICU length of stay
Time Frame
90 days
Title
Time on mechanical ventilation
Description
Time on mechanical ventilation
Time Frame
10 days
Title
Cumulative catecholamine dose
Description
Cumulative catecholamine dose
Time Frame
10 days
Title
Overall and ICU mortality
Description
Overall and ICU mortality
Time Frame
90 days
Title
Serum levels of administered anti-infectives
Description
Serum drug Levels of pre and post filter and adsorber system on day 1-3 while CytoSorb therapy (sampling: t 0, 1, 2, 6, 8, 12, 24 h after CytoSorb initiation)
Time Frame
3 days
Title
Change of plasma Interleukin-6 (IL6) level
Description
Change of plasma Interleukin-6 (IL6) level
Time Frame
10 days
Title
Change of plasma Interleukin-10 (IL10) level
Description
Change of plasma Interleukin-10 (IL10) level
Time Frame
10 days
Title
Change of plasma Procalcitonin (PCT) level
Description
Change of plasma Procalcitonin (PCT) level
Time Frame
10 days
Title
Change of HLA-DR level
Description
Change of HLA-DR (Human Leukocyte Antigen - DR isotype) level of monocytes
Time Frame
10 days
Title
Change of TNF alpha level after ex-vivo stimulation
Description
Change of TNF-alfa level (Tumor Necrosis Factor alpha) level after LPS (Lipopolysaccharides) stimulation as sign of monocytic immunocompetence
Time Frame
10 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:
Refractory septic shock
Need for Norepinephrine ≥ 0.25 µg/kg/min
IL6 ≥ 1000 ng/l
Indication for CRRT
Exclusion Criteria:
Sepsis due to pulmonary or urogenital causes
Onset of septic shock longer than 36 hours
Liver cirrhosis Child Pugh C
"do not resuscitate"-order
expected survival < 14 days
participation in another interventional trial
Pregnancy or breastfeeding
Lack of consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dominik Jarczak, MD
Phone
+49 40 741035315
Email
d.jarczak@uke.de
First Name & Middle Initial & Last Name or Official Title & Degree
Axel Nierhaus, MD
Phone
+49 40 741035315
Email
nierhaus@uke.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stefan Kluge, MD
Organizational Affiliation
University Hospital Hamburg-Eppendorf, Department of Intensive Care Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Hamburg-Eppendorf
City
Hamburg
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dominik Jarczak, MD
Phone
+49 40 741035315
Email
d.jarczak@uke.de
First Name & Middle Initial & Last Name & Degree
Axel Nierhaus, MD
Phone
+49 40 741035315
Email
nierhaus@uke.de
First Name & Middle Initial & Last Name & Degree
Stefan Kluge, MD
First Name & Middle Initial & Last Name & Degree
Dominik Jarczak, MD
First Name & Middle Initial & Last Name & Degree
Axel Nierhaus, MD
First Name & Middle Initial & Last Name & Degree
Christina König, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28537517
Citation
Taeb AM, Hooper MH, Marik PE. Sepsis: Current Definition, Pathophysiology, Diagnosis, and Management. Nutr Clin Pract. 2017 Jun;32(3):296-308. doi: 10.1177/0884533617695243. Epub 2017 Mar 17.
Results Reference
background
PubMed Identifier
28589286
Citation
Friesecke S, Stecher SS, Gross S, Felix SB, Nierhaus A. Extracorporeal cytokine elimination as rescue therapy in refractory septic shock: a prospective single-center study. J Artif Organs. 2017 Sep;20(3):252-259. doi: 10.1007/s10047-017-0967-4. Epub 2017 Jun 6.
Results Reference
background
PubMed Identifier
30481999
Citation
Garau I, Marz A, Sehner S, Reuter DA, Reichenspurner H, Zollner C, Kubitz JC. Hemadsorption during cardiopulmonary bypass reduces interleukin 8 and tumor necrosis factor alpha serum levels in cardiac surgery: a randomized controlled trial. Minerva Anestesiol. 2019 Jul;85(7):715-723. doi: 10.23736/S0375-9393.18.12898-7. Epub 2018 Nov 22.
Results Reference
background
PubMed Identifier
28343448
Citation
Kogelmann K, Jarczak D, Scheller M, Druner M. Hemoadsorption by CytoSorb in septic patients: a case series. Crit Care. 2017 Mar 27;21(1):74. doi: 10.1186/s13054-017-1662-9.
Results Reference
background
PubMed Identifier
22903091
Citation
Bayer O, Reinhart K, Kohl M, Kabisch B, Marshall J, Sakr Y, Bauer M, Hartog C, Schwarzkopf D, Riedemann N. Effects of fluid resuscitation with synthetic colloids or crystalloids alone on shock reversal, fluid balance, and patient outcomes in patients with severe sepsis: a prospective sequential analysis. Crit Care Med. 2012 Sep;40(9):2543-51. doi: 10.1097/CCM.0b013e318258fee7.
Results Reference
background
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Adjuvant Therapy With CytoSorb in Refractory Septic Shock
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