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The Effects of Oxiris on Systemic Inflammation and Endothelial dysFunction (EOSIEF)

Primary Purpose

Acute Kidney Injury Due to Circulatory Failure (Disorder)

Status
Unknown status
Phase
Not Applicable
Locations
Russian Federation
Study Type
Interventional
Intervention
oXiris membrane
Sponsored by
St. Petersburg State Pavlov Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Kidney Injury Due to Circulatory Failure (Disorder) focused on measuring acute kidney injury

Eligibility Criteria

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

Inclusion Criteria:

  • elective cardiac surgery patients undergoing CPB (>60 minutes) with valve replacement and CABG.

Exclusion Criteria:

  • Immunosuppressive therapy, CKD 4 and 5 stages, RRT in last 90 days, pregnancy, autoimmune disease, allergy to heparin.

Sites / Locations

  • Pavlov First St. Petersburg State Medical UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

patients undergoing CRRT with oXiris membrane

standard protocol

Arm Description

Elective cardiac surgery patients undergoing CPB we will range in 2 groups: I- with Prismaflex set oXiris (SCUF) after CPB, II- standard protocol. Indications for CRRT (SCUF) with oXiris after ICU admission: 1. Signs of pulmonary edema after cardiac surgery, verified with X-ray control. Or high risk of pulmonary edema after cardiac surgery: Fluid overload ≥ 10%, measured with equation (%fluid overload= ((total fluid in- total fluid out)/admission body weight*100) CVP (central venous pressure) ˃ 12 mm H2O. PAWP (pulmonary arterial wedge pressure) ˃ 12 mm Hg, measured by Swan-Ganz catheter. In this arm the treatment of fluid overload will be provided via SCUF with oxiris membrane

Elective cardiac surgery patients undergoing CPB we will range in 2 groups: I- with Prismaflex set oXiris (SCUF) after CPB, II- standard protocol. Indications for CRRT (SCUF) with oXiris after ICU admission: 1. Signs of pulmonary edema after cardiac surgery, verified with X-ray control. Or high risk of pulmonary edema after cardiac surgery: Fluid overload ≥ 10%, measured with equation (%fluid overload= ((total fluid in- total fluid out)/admission body weight*100) CVP (central venous pressure) ˃ 12 mm H2O. PAWP (pulmonary arterial wedge pressure) ˃ 12 mm Hg, measured by Swan-Ganz catheter. In this arm the management of fluid overload will be provided via diuretics or IHD (in condition diuretics treatment resistance)

Outcomes

Primary Outcome Measures

Patient volume status assessment in perioperative period
To compare volume status in two arms based on CVP mmH2O and PAWP mmHg measurements

Secondary Outcome Measures

survival after cardiac surgery
to compare in arms with oxiris treatment and standard protocol amount of survived patients
'ICU and hospital length of stay after cardiac surgery.
to compare in arms with oxiris treatment and standard protocol the amount of days spent in ICU wards and in hospital

Full Information

First Posted
January 17, 2020
Last Updated
August 31, 2020
Sponsor
St. Petersburg State Pavlov Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04257006
Brief Title
The Effects of Oxiris on Systemic Inflammation and Endothelial dysFunction
Acronym
EOSIEF
Official Title
The Effects of oXiris on Systemic Inflammation, Endothelial Dysfunction and Volume Control in Cardiac Surgery Patients Undergoing Cardiopulmonary Bypass.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 17, 2020 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
June 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Petersburg State Pavlov Medical University

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
CS-AKI occurring in 20% to 70% of cases depending of the type of cardiac surgery. The systemic inflammatory response is often observed and associated with increased risk of AKI. Cardiopulmonary bypass (CPB) induces a complex inflammatory response that has a multifactorial pathogenesis. The inflammatory response is triggered by exposure of the blood to artificial surfaces during extracorporeal circulation, ischemia/reperfusion injuries, translocation of gram-negative bacteria from the intestinal tract, small amounts of LPS in IV solutions. SIRS during CPB with high levels of inflammatory mediators, active complement proteins and LPS provoke endothelial dysfunction- retraction of endothelial cells with increasing vascular permeability and thrombogenic activity, also inflammatory mediators activate leukocytes and they enhance vascular permeability by affecting endothelial cells and vascular basement membrane. The systemic inflammation and endothelial dysfunction are the basis for multiple organ dysfunction syndrome. Vascular integrity damage during cardiac surgery entail redistribution of fluids with interstitial fluid accumulation and require accurate volume control (pertinent removal of "CPB priming volume"), especially in patients with CKD (low GFR) with high risks of AKI.
Detailed Description
Specific details of Treatment/Intervention: (prescription and/or therapy, devices, equipment, solutions, product to be used in conducting study: To apply Prismaflex system with oXiris membrane after cardiopulmonary bypass in SCUF modality for CPB priming volume elimination. Duration of procedure: 6 hours Blood flow:150-200 ml/min Anticoagulation: no additional heparinization. According to the features of oXiris membrane: Cytokines, complement, endotoxin adsorptive capacity. Capability of accurate fluid balance management after cardiac surgery and CPB. Reduced demand of anticoagulation therapy for CRRT in patients with high risk of bleeding. The goal of the research: To evaluate effect of adsorption of oXiris membrane on levels of complement (C3a, C5a), pro- and anti-inflammatory cytokines (IL-1β, TNF-α,IL-6,Il-8, IL-10,TGF-β), LPS (EAA levels) after CPB. To evaluate leukocytes activation after CPB and after inflammatory mediators adsorption with oXiris (CD11b/CD18) To evaluate endothelial dysfunction after CPB and after CRRT with oXiris: endothelial/leukocytes interactions (ICAM-1, VCAM-1), biomarkers of endothelial permeability (angiopoetin-2, sFLT-1), biomarkers of endothelial coagulopathy (von Willebrand factor, thrombomodulin) To evaluate effect of volume control with CRRT on CS-AKI and dependence on mechanical ventilation after cardiac surgery, regarding volume overload in patients undergoing CPB with "priming volume" infusion. To evaluate stage and topography of cardiac surgery associated acute kidney injury (creatinine, cystatin C, NGAL, KIM-1, β2-microglobuline) in patients in two arms: oXiris and standard protocol. To evaluate adsorptive and volume control feasible effects of oXiris membrane on volume management (CVP,PAWP), LPS adsorption, reduction of systemic inflammation , endothelium dysfunction and AKI after cardiac surgery with CPB in comparison with standard protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury Due to Circulatory Failure (Disorder)
Keywords
acute kidney injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
patients undergoing CRRT with oXiris membrane
Arm Type
Experimental
Arm Description
Elective cardiac surgery patients undergoing CPB we will range in 2 groups: I- with Prismaflex set oXiris (SCUF) after CPB, II- standard protocol. Indications for CRRT (SCUF) with oXiris after ICU admission: 1. Signs of pulmonary edema after cardiac surgery, verified with X-ray control. Or high risk of pulmonary edema after cardiac surgery: Fluid overload ≥ 10%, measured with equation (%fluid overload= ((total fluid in- total fluid out)/admission body weight*100) CVP (central venous pressure) ˃ 12 mm H2O. PAWP (pulmonary arterial wedge pressure) ˃ 12 mm Hg, measured by Swan-Ganz catheter. In this arm the treatment of fluid overload will be provided via SCUF with oxiris membrane
Arm Title
standard protocol
Arm Type
No Intervention
Arm Description
Elective cardiac surgery patients undergoing CPB we will range in 2 groups: I- with Prismaflex set oXiris (SCUF) after CPB, II- standard protocol. Indications for CRRT (SCUF) with oXiris after ICU admission: 1. Signs of pulmonary edema after cardiac surgery, verified with X-ray control. Or high risk of pulmonary edema after cardiac surgery: Fluid overload ≥ 10%, measured with equation (%fluid overload= ((total fluid in- total fluid out)/admission body weight*100) CVP (central venous pressure) ˃ 12 mm H2O. PAWP (pulmonary arterial wedge pressure) ˃ 12 mm Hg, measured by Swan-Ganz catheter. In this arm the management of fluid overload will be provided via diuretics or IHD (in condition diuretics treatment resistance)
Intervention Type
Device
Intervention Name(s)
oXiris membrane
Intervention Description
Open heart surgery patients in early postoperative period with clinical signs of fluid overload undergoing CRRT
Primary Outcome Measure Information:
Title
Patient volume status assessment in perioperative period
Description
To compare volume status in two arms based on CVP mmH2O and PAWP mmHg measurements
Time Frame
in 24 hours
Secondary Outcome Measure Information:
Title
survival after cardiac surgery
Description
to compare in arms with oxiris treatment and standard protocol amount of survived patients
Time Frame
in 90 day
Title
'ICU and hospital length of stay after cardiac surgery.
Description
to compare in arms with oxiris treatment and standard protocol the amount of days spent in ICU wards and in hospital
Time Frame
in 28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: elective cardiac surgery patients undergoing CPB (>60 minutes) with valve replacement and CABG. Exclusion Criteria: Immunosuppressive therapy, CKD 4 and 5 stages, RRT in last 90 days, pregnancy, autoimmune disease, allergy to heparin.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yury Polushin, PhD
Phone
+7 (812) 338-66-49
Email
polushin1@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Dmitry Sokolov, MD
Phone
+7(911)7193333
Email
sokolovdv82@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yury Polushin, PhD
Organizational Affiliation
Pavlov First St. Petersburg State Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pavlov First St. Petersburg State Medical University
City
Saint Petersburg
State/Province
Russsia
ZIP/Postal Code
197022
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yury Polushin, PhD
Phone
+78123387823
Email
polushin1@gmail.com
First Name & Middle Initial & Last Name & Degree
Dmitry Sokolov, MD
Phone
+79117193333
Email
sokolovdv82@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
de-identified individual participant data for all primary and secondary outcome measures will be made available
IPD Sharing Time Frame
data will be available within 1 year of study completion
IPD Sharing Access Criteria
data access request will be reviewed by an external independent review panel.
IPD Sharing URL
http://1spbgmu.ru

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The Effects of Oxiris on Systemic Inflammation and Endothelial dysFunction

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