Cytokine Clearance With Cytoabsorbant Device During Cardiac Bypass (CCCC)
Primary Purpose
Myocardial Ischemia, Heart Valve Diseases
Status
Completed
Phase
Phase 1
Locations
Switzerland
Study Type
Interventional
Intervention
Cytosorb
Sponsored by
About this trial
This is an interventional prevention trial for Myocardial Ischemia
Eligibility Criteria
Inclusion Criteria:
Patients planned for elective cardiac surgery requiring CPB and (≥1 among):
- Age >75 years' old AND / OR
- Double valvular replacement AND / OR
- Complex surgery with expected CPB time >120 min AND / OR
- Redo cardiac surgery AND / OR
- Pre-op chronic renal failure (GFR<30 ml/min) AND / OR Chronic heart failure (LVEF <40%)
Exclusion Criteria:
- End stage renal disease (dialysis dependence)
- Emergency procedure
- Active infectious endocarditis
- Off-pump procedure planned
- Non steroidal anti-inflammatory treatment in the previous 7 days
- Corticosteroids administration in the previous 7 days
- No informed consent
- Enrolment in another conflicting study
Sites / Locations
- Centre Hospitalier Universitaire Vaudois
Arms of the Study
Arm 1
Arm 2
Arm Type
No Intervention
Experimental
Arm Label
Control
Cytosorb
Arm Description
Conventional cardio-pulmonary bypass
Cytosorb added to cardio-pulmonary bypass
Outcomes
Primary Outcome Measures
Change in Cytokine levels
Secondary Outcome Measures
Change in Cytokine levels
Change in Cytokine levels
Change in Coagulation factors serum levels
Duration of the need for vasopressors
Duration of mechanical ventilation
ICU length of stay
Hospital Length of stay
In-hospital mortality
Full Information
NCT ID
NCT02775123
First Posted
April 21, 2016
Last Updated
January 23, 2018
Sponsor
Centre Hospitalier Universitaire Vaudois
1. Study Identification
Unique Protocol Identification Number
NCT02775123
Brief Title
Cytokine Clearance With Cytoabsorbant Device During Cardiac Bypass
Acronym
CCCC
Official Title
Cytokine Clearance With Cytoabsorbant Device During Cardiac Bypass: a Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
May 2016 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
January 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre Hospitalier Universitaire Vaudois
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Investigators are planning a single center pilot randomized controlled trial to assess the potential of a Cytoadsorbant filter (Cytosorb®, Germany) to remove cytokines from the blood during cardiac surgery.
Investigators will screen all patients undergoing cardiac surgery and approach those deemed at risk of post surgical complications [≥ 1 among: age >75 years old, double valvular replacement, complex surgery with expected CPB time >100 min, redo cardiac surgery, pre-op chronic renal failure (plasma creatinine level >120 mcmol/l) or chronic heart failure (LVEF <35%)].
Patients with end-stage renal disease (dialysis dependence), undergoing an emergency procedure or an off-pump procedure, those who decline informed consent as well as those enrolled in another conflicting study will be excluded.
Eligible patients will be approached, consented and enrolled in the trial. Patients will then be randomized to either receive conventional CPB (control arm) or CPB plus Cytosorb (intervention arm). The target population is 30 patients (15 per arm).
For this pilot study, investigators main outcome will be differences between the two arms in measurement of serum levels for IL-2, IL-6, IL-10 and TNF alpha at baseline (pre-operatively), on ICU admission, as well as 6 and 24 hrs post CPB.
Secondary outcomes will be changes in coagulation factors serum levels, the need for vasopressors, inotropes, mechanical ventilation and renal replacement therapy, ICU and hospital length of stay as well as in-hospital mortality.
Recruitment period should span from May 2016 to April 2017.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myocardial Ischemia, Heart Valve Diseases
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control
Arm Type
No Intervention
Arm Description
Conventional cardio-pulmonary bypass
Arm Title
Cytosorb
Arm Type
Experimental
Arm Description
Cytosorb added to cardio-pulmonary bypass
Intervention Type
Device
Intervention Name(s)
Cytosorb
Intervention Description
A cytoadsorbent cardridge (Cytosorb) will be added to the extra-corporeal circuit (CPB).
Primary Outcome Measure Information:
Title
Change in Cytokine levels
Time Frame
From Baseline (Preoeratively) to 6hrs post CPB
Secondary Outcome Measure Information:
Title
Change in Cytokine levels
Time Frame
From Baseline (Preoeratively) to 24 hrs post CPB
Title
Change in Cytokine levels
Time Frame
From Baseline (Preoeratively) to end of CPB
Title
Change in Coagulation factors serum levels
Time Frame
From baseline (pre-operatively) to end of CPB as well as 6 hrs and 24 hrs post CPB
Title
Duration of the need for vasopressors
Time Frame
28 days
Title
Duration of mechanical ventilation
Time Frame
28 days
Title
ICU length of stay
Time Frame
90 days
Title
Hospital Length of stay
Time Frame
90 days
Title
In-hospital mortality
Time Frame
90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients planned for elective cardiac surgery requiring CPB and (≥1 among):
Age >75 years' old AND / OR
Double valvular replacement AND / OR
Complex surgery with expected CPB time >120 min AND / OR
Redo cardiac surgery AND / OR
Pre-op chronic renal failure (GFR<30 ml/min) AND / OR Chronic heart failure (LVEF <40%)
Exclusion Criteria:
End stage renal disease (dialysis dependence)
Emergency procedure
Active infectious endocarditis
Off-pump procedure planned
Non steroidal anti-inflammatory treatment in the previous 7 days
Corticosteroids administration in the previous 7 days
No informed consent
Enrolment in another conflicting study
Facility Information:
Facility Name
Centre Hospitalier Universitaire Vaudois
City
Lausanne
State/Province
Vaud
ZIP/Postal Code
1011
Country
Switzerland
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30944029
Citation
Poli EC, Alberio L, Bauer-Doerries A, Marcucci C, Roumy A, Kirsch M, De Stefano E, Liaudet L, Schneider AG. Cytokine clearance with CytoSorb(R) during cardiac surgery: a pilot randomized controlled trial. Crit Care. 2019 Apr 3;23(1):108. doi: 10.1186/s13054-019-2399-4.
Results Reference
derived
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Cytokine Clearance With Cytoabsorbant Device During Cardiac Bypass
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