Extracorporeal Elimination of Cytokines Following Abdominal-thoracic Esophagectomy (EXCESS)
Primary Purpose
Inflammation
Status
Terminated
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
CytoSorb cytokine elimination
Sponsored by
About this trial
This is an interventional treatment trial for Inflammation focused on measuring Esophagectomy Inflammation Hemoperfusion Cytokines
Eligibility Criteria
Inclusion Criteria:
- abdominal-thoracic esophagectomy with radical lymphadenectomy
- post operative admission to ICU
- age >= 18 yrs
- written informed consent
Exclusion Criteria:
- Participation in another interventional trial
- pregnancy or lactation
- systemic medication with high dose steroids and/or immunosuppressants and/or radiotherapy during the last 3 months
- known diseases of the immune system (benign and malign)
- contraindications for extracorporeal therapy
- Thrombocytopenia < 50*10^9/l
- therapy limitations (DNR), moribund status
- missing informed consent
Sites / Locations
- University Medical Center Hamburg-Eppendorf
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Standard Care
CytoSorb
Arm Description
intensive care therapy according to international standards and following local SOPs, including fluid therapy, mechanical ventilation, catecholamine therapy and other pharmacotherapy as required
all of the above, plus extracorporeal hemadsorption therapy (CytoSorbents Adsorber cartridge) using continuous veno-venous hemofiltration (citrate anticoagulation) CytoSorb cytokine elimination
Outcomes
Primary Outcome Measures
Change of interleukin-6 plasma levels
Change of interleukin-6 plasma levels
Secondary Outcome Measures
Change in SOFA Score
decrease of >= 2 score points in the intervention group
Change of catecholamine dose
decrease of >= 0.1 µg/kg/min catecholamine dosage to achieve MAP > 65 mmHg in intervention group
Fluid intake
reduction of fluid intake to maintain MAP > 65 mmHg of >= 1000 ml/24h in intervention group
Full Information
NCT ID
NCT02606799
First Posted
October 1, 2015
Last Updated
June 29, 2022
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
CytoSorbents, Inc
1. Study Identification
Unique Protocol Identification Number
NCT02606799
Brief Title
Extracorporeal Elimination of Cytokines Following Abdominal-thoracic Esophagectomy
Acronym
EXCESS
Official Title
Extracorporeal Elimination of Cytokines Following Abdominal-thoracic Esophagectomy - a Randomized Study (EXCESS)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Terminated
Why Stopped
No further recruitment possible due to changed conditions
Study Start Date
May 2016 (Actual)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
April 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
CytoSorbents, Inc
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study evaluates the effect of extracorporeal removal of inflammatory mediators on the systemic inflammation reaction of patients admitted to the intensive care unit following elective esophagectomy. Half of the participants will be treated with an adsorption device (CytoSorbents Adsorber), while the other half will be treated according to standard care. Significant reductions of interleukin-6 plasma concentration, SOFA score and catecholamine dosage in the intervention group are expected.
Detailed Description
Radical esophagectomy combined with extensive lymphadenectomy for esophageal cancer is one of the most invasive surgical procedures. Even with progress made in surgical technique and postoperative management the rate of short- and long term complications remains high. The surgical trauma invariably causes liberation and activation of inflammatory mediators and danger associated molecular patterns, which in turn result in a pronounced systemic inflammatory reaction, leading to multiorgan dysfunction including adult respiratory distress syndrome (ARDS) in many patients. The subsequent counter regulation of the immune system induces immune paralysis, which is followed by infectious complications and increases the probability of severe sepsis. Moreover, severe systemic inflammation causes capillary leakage, resulting in impaired wound healing and endangered anastomoses.
Therefore, it seems that early and effective measures against the excessive production of mediators and cytokines are indicated without impairment of the innate and adaptive immune response as it would be expected with the administration of e.g. steroids. Instead, the removal of an excessive amount of circulating cytokines might be a desirable method having shown its effectivity in the therapy of septic shock in the past.
The aim of this study is to demonstrate the effectiveness of extracorporeal cytokine removal to dampen the systemic inflammatory response following abdominal-thoracic esophagectomy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammation
Keywords
Esophagectomy Inflammation Hemoperfusion Cytokines
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
intensive care therapy according to international standards and following local SOPs, including fluid therapy, mechanical ventilation, catecholamine therapy and other pharmacotherapy as required
Arm Title
CytoSorb
Arm Type
Experimental
Arm Description
all of the above, plus extracorporeal hemadsorption therapy (CytoSorbents Adsorber cartridge) using continuous veno-venous hemofiltration (citrate anticoagulation) CytoSorb cytokine elimination
Intervention Type
Device
Intervention Name(s)
CytoSorb cytokine elimination
Other Intervention Name(s)
hemadsorption
Intervention Description
Hemoperfusion using continuous veno-venous hemofiltration (citrate regional anticoagulation) with CytoSorb cytokine elimination over a period of 48h immediately following admission to the intensive care unit
Primary Outcome Measure Information:
Title
Change of interleukin-6 plasma levels
Description
Change of interleukin-6 plasma levels
Time Frame
72 hours
Secondary Outcome Measure Information:
Title
Change in SOFA Score
Description
decrease of >= 2 score points in the intervention group
Time Frame
120 hours
Title
Change of catecholamine dose
Description
decrease of >= 0.1 µg/kg/min catecholamine dosage to achieve MAP > 65 mmHg in intervention group
Time Frame
48 hours
Title
Fluid intake
Description
reduction of fluid intake to maintain MAP > 65 mmHg of >= 1000 ml/24h in intervention group
Time Frame
120 hours
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
abdominal-thoracic esophagectomy with radical lymphadenectomy
post operative admission to ICU
age >= 18 yrs
written informed consent
Exclusion Criteria:
Participation in another interventional trial
pregnancy or lactation
systemic medication with high dose steroids and/or immunosuppressants and/or radiotherapy during the last 3 months
known diseases of the immune system (benign and malign)
contraindications for extracorporeal therapy
Thrombocytopenia < 50*10^9/l
therapy limitations (DNR), moribund status
missing informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Axel Nierhaus, MD
Organizational Affiliation
University Medical Center Hamburg-Eppendorf, Dep. of Critical Care
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Medical Center Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20251
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
22027760
Citation
Panagiotou A, Gaiao S, Cruz DN. Extracorporeal therapies in sepsis. J Intensive Care Med. 2013 Sep-Oct;28(5):281-95. doi: 10.1177/0885066611425759. Epub 2011 Oct 25.
Results Reference
background
PubMed Identifier
25656010
Citation
Bruenger F, Kizner L, Weile J, Morshuis M, Gummert JF. First successful combination of ECMO with cytokine removal therapy in cardiogenic septic shock: a case report. Int J Artif Organs. 2015 Feb;38(2):113-6. doi: 10.5301/ijao.5000382. Epub 2015 Feb 3.
Results Reference
background
PubMed Identifier
15090965
Citation
Kellum JA, Song M, Venkataraman R. Hemoadsorption removes tumor necrosis factor, interleukin-6, and interleukin-10, reduces nuclear factor-kappaB DNA binding, and improves short-term survival in lethal endotoxemia. Crit Care Med. 2004 Mar;32(3):801-5. doi: 10.1097/01.ccm.0000114997.39857.69.
Results Reference
background
PubMed Identifier
25538418
Citation
Basu R, Pathak S, Goyal J, Chaudhry R, Goel RB, Barwal A. Use of a novel hemoadsorption device for cytokine removal as adjuvant therapy in a patient with septic shock with multi-organ dysfunction: A case study. Indian J Crit Care Med. 2014 Dec;18(12):822-4. doi: 10.4103/0972-5229.146321.
Results Reference
background
PubMed Identifier
23920222
Citation
Mitzner SR, Gloger M, Henschel J, Koball S. Improvement of hemodynamic and inflammatory parameters by combined hemoadsorption and hemodiafiltration in septic shock: a case report. Blood Purif. 2013;35(4):314-5. doi: 10.1159/000351206. Epub 2013 Jul 31. No abstract available.
Results Reference
background
Links:
URL
http://cytosorb-therapy.com/
Description
technical and scientific information
Learn more about this trial
Extracorporeal Elimination of Cytokines Following Abdominal-thoracic Esophagectomy
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