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Hemadsorption During and After Cardiopulmonary Bypass to Modulate the Inflammatory Response (IMHeS)

Primary Purpose

Inflammatory Response, Chronic Renal Disease, Cardiac Surgery

Status
Unknown status
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
CytoSorb
Control
Sponsored by
University Magna Graecia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Inflammatory Response focused on measuring hemadsorption

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All consecutive adult patients (age >65 years) undergoing cardiac surgery with an anticipated CPB time duration longer than 60 minutes.
  • Presence of CKD defined by a Glomerular Filtration Rate (eGFR) < 60 ml/min/1.73 m2.
  • Consent to participate to the study

Exclusion Criteria:

  • emergency surgery
  • acute infective endocarditis
  • systemic infectious diseases
  • previous kidney transplant
  • need for contrast enhancement during surgery
  • immunosuppressive or long-term corticosteroid therapies
  • participation to other investigations.

Sites / Locations

  • AOU Mater Domini

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

CytoSorb

Control

Arm Description

Patients assigned to this arm group will receive hemadsorption witbhCytoSorb during the surgery and in the next 24 hours after surgery.

Patients assigned to this arm group will undergo to a normal CPB without the use of any hemoadsorption system.

Outcomes

Primary Outcome Measures

IL-6 concentration at ICU admission
Investigators will assess the blood IL-6 concentrations between the two arms

Secondary Outcome Measures

IL-6 concentration before cardiac surgery
Investigators will assess the blood IL-6 concentrations between the two arms
IL-6 concentration at the end of CardioPulmonary Bypass
Investigators will assess the blood IL-6 concentrations between the two arms
IL-6 concentration 2 hours after the end of CardioPulmonary Bypass
Investigators will assess the blood IL-6 concentrations between the two arms
IL-6 concentration 48 hours after the end of CardioPulmonary Bypass
Investigators will assess the blood IL-6 concentrations between the two arms
Renal function
Investigators will assess the blood creatinine concentrations in the two arms
Myoglobin concentration
Investigators will assess the blood myoglobin concentrations in the two arms
Haptoglobin concentration
Investigators will assess the blood haptoglobin concentrations in the two arms
Liver transaminases concentration
Investigators will measure the liver transaminases concentrations in the two arms to assess any liver injury
Osteopontin concentration
Investigators will measure the osteopontin concentrations in the two arms to assess the inflammatory status
Free hemoglobin concentration
Investigators will assess the free hemoglobin concentrations in the two arms

Full Information

First Posted
October 13, 2019
Last Updated
November 10, 2020
Sponsor
University Magna Graecia
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1. Study Identification

Unique Protocol Identification Number
NCT04157647
Brief Title
Hemadsorption During and After Cardiopulmonary Bypass to Modulate the Inflammatory Response
Acronym
IMHeS
Official Title
Monocentric Prospective Randomized Pilot Study in Patients With Kidney Failure to Evaluate the Relationship Between the Hemadsorption During and After Cardiopulmonary Bypass and the Modulation of Post-surgical Inflammatory Response
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 15, 2020 (Anticipated)
Primary Completion Date
November 1, 2021 (Anticipated)
Study Completion Date
November 15, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Magna Graecia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic kidney disease (CKD) is a risk factor for the development of cardiovascular disease, which increases the risk of death after cardiac surgery. High interleukin 6 (IL-6) blood levels is commonly observed in patients with CKD, and this is particularly high after cardiac surgery. High IL-6 levels are also associated with increased long-term mortality rate after cardiac surgery. To date, the use of ultrafiltration or endotoxin adsorption systems were not found to improve the clinical outcome, although able to reduce the inflammatory mediators concentrations. In the last years, a new extracorporeal hemadsorption filter (CytoSorb) has been developed for removal of inflammatory cytokines and it has been approved by the European Union. However, data lack about the impact on clinical outcome of the use of CytoSorb in patients with CKD undergoing cardiac surgery with cardio-pulmonary bypass (CPB). The investigators have therefore designed this pilot prospective randomized trial to evaluate the efficacy the intraoperative use of CytoSorb for cytokines removal to prevent the inflammatory response associated with the cardiac surgery and complications in patients with CKD.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Response, Chronic Renal Disease, Cardiac Surgery
Keywords
hemadsorption

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CytoSorb
Arm Type
Active Comparator
Arm Description
Patients assigned to this arm group will receive hemadsorption witbhCytoSorb during the surgery and in the next 24 hours after surgery.
Arm Title
Control
Arm Type
Sham Comparator
Arm Description
Patients assigned to this arm group will undergo to a normal CPB without the use of any hemoadsorption system.
Intervention Type
Device
Intervention Name(s)
CytoSorb
Intervention Description
The hemadsorption filter will be included in the CPB circuit between the oxygenator and the venous reservoir. After cardiac surgery, the use of the filter will be continued till 24 hours after the end of surgery.
Intervention Type
Device
Intervention Name(s)
Control
Intervention Description
No hemadsorption filter or other treatment will be included in the CPB circuit
Primary Outcome Measure Information:
Title
IL-6 concentration at ICU admission
Description
Investigators will assess the blood IL-6 concentrations between the two arms
Time Frame
At day 0 after surgery
Secondary Outcome Measure Information:
Title
IL-6 concentration before cardiac surgery
Description
Investigators will assess the blood IL-6 concentrations between the two arms
Time Frame
At day 0 before the cardiac surgery
Title
IL-6 concentration at the end of CardioPulmonary Bypass
Description
Investigators will assess the blood IL-6 concentrations between the two arms
Time Frame
At day 0 at the end of the CardioPulmonary Bypass
Title
IL-6 concentration 2 hours after the end of CardioPulmonary Bypass
Description
Investigators will assess the blood IL-6 concentrations between the two arms
Time Frame
2 hours after the end of CardioPulmonary Bypass
Title
IL-6 concentration 48 hours after the end of CardioPulmonary Bypass
Description
Investigators will assess the blood IL-6 concentrations between the two arms
Time Frame
48 hours after the end of CardioPulmonary Bypass
Title
Renal function
Description
Investigators will assess the blood creatinine concentrations in the two arms
Time Frame
daily up to day 15
Title
Myoglobin concentration
Description
Investigators will assess the blood myoglobin concentrations in the two arms
Time Frame
daily up to day 15
Title
Haptoglobin concentration
Description
Investigators will assess the blood haptoglobin concentrations in the two arms
Time Frame
daily up to day 15
Title
Liver transaminases concentration
Description
Investigators will measure the liver transaminases concentrations in the two arms to assess any liver injury
Time Frame
daily up to day 15
Title
Osteopontin concentration
Description
Investigators will measure the osteopontin concentrations in the two arms to assess the inflammatory status
Time Frame
daily up to day 15
Title
Free hemoglobin concentration
Description
Investigators will assess the free hemoglobin concentrations in the two arms
Time Frame
daily up to day 15

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All consecutive adult patients (age >65 years) undergoing cardiac surgery with an anticipated CPB time duration longer than 60 minutes. Presence of CKD defined by a Glomerular Filtration Rate (eGFR) < 60 ml/min/1.73 m2. Consent to participate to the study Exclusion Criteria: emergency surgery acute infective endocarditis systemic infectious diseases previous kidney transplant need for contrast enhancement during surgery immunosuppressive or long-term corticosteroid therapies participation to other investigations.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Giuseppe F Serraino, MD
Phone
0039 0961 3647033
Email
filiberto@live.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Giuseppe Serraino, MD
Organizational Affiliation
Magna Graecia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
AOU Mater Domini
City
Catanzaro
State/Province
CZ
ZIP/Postal Code
88100
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The full protocol, datasets used and analysed during the current study will be available on reasonable request after study publication
IPD Sharing Time Frame
After scientific publication
IPD Sharing Access Criteria
On reasonable request
Citations:
PubMed Identifier
16738019
Citation
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PubMed Identifier
10843245
Citation
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PubMed Identifier
12234313
Citation
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PubMed Identifier
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Hemadsorption During and After Cardiopulmonary Bypass to Modulate the Inflammatory Response

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