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Prevention of Renal Failure by Nitric Oxide in Prolonged Cardiopulmonary Bypass.

Primary Purpose

Heart Valve Diseases, Heart; Complications, Valve, Prosthesis, Cardiac Valve Replacement Complication

Status
Completed
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
inhaled nitric oxide
inhaled Nitrogen
Sponsored by
Xijing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Heart Valve Diseases

Eligibility Criteria

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

Inclusion Criteria:

  • Provide written informed consent
  • Are > 18 years of age
  • Elective cardiac or aortic surgery with CPB, when the surgeon plans double valve replacement.
  • Stable pre-operative renal function, without dialysis.

Exclusion Criteria:

  • Emergent cardiac surgery
  • Life expectancy < 1 year
  • Hemodynamic instability as defined by a systolic blood pressure <90 mmHg
  • Administration of ≥1 Packed Red Blood Cell transfusion in the week before surgery
  • X-ray contrast infusion less than 1 week before surgery
  • Anticipate administration of nephrotoxic agents, such as hydroxyethyl starch
  • Evidence of intravascular or extravascular hemolysis

Sites / Locations

  • Xijing Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

inhaled nitrogen

inhaled nitric oxide

Arm Description

Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, pure nitrogen (placebo) is mixed with pure O2 or air. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the NO is delivered through the inspiratory limb of the anesthetic or ventilator circuit.

Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, 800 ppm NO gas is mixed with pure O2 or air to obtain a final concentration of 80 ppm NO. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the gas is delivered through the inspiratory limb of the anesthetic or ventilator circuit. NO, NO2 and O2 and methemoglobin levels are monitored by an unblinded observer.

Outcomes

Primary Outcome Measures

acute kidney injury
acute kidney injury was defined by the KDIGO criteria

Secondary Outcome Measures

Chronic kidney disease
defined as eGFR<60 mL/min/1.73m2
Loss of 25% of eGFR compared to baseline
Loss of 25% of eGFR compared to baseline
Major adverse kidney events (MAKE)
a composite outcome of loss of 25% of eGFR from baseline, end stage renal disease requiring a continuous renal replacement therapy and mortality.
Renal Replacement Therapy
the incidence of need for Renal Replacement Therapy
Incidence of nonfatal stroke and nonfatal myocardial infarction.
Nonfatal stroke will be assessed by the NIH Stroke Scale at baseline before surgery and at 28 days, 60 days, 90 days and 1 year after surgery. Nonfatal myocardial infarction is defined by the third universal definition of MI released in 2012 by the ESC/ACCF/AHA/WHF.
Quality of life
The quality of life will be evaluated by the Katz Index of In dependence in Activities of Daily living
overall mortality
all cause mortality

Full Information

First Posted
February 25, 2013
Last Updated
February 10, 2018
Sponsor
Xijing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01802619
Brief Title
Prevention of Renal Failure by Nitric Oxide in Prolonged Cardiopulmonary Bypass.
Official Title
Prevention of Renal Failure by Nitric Oxide in Prolonged Cardiopulmonary Bypass: A Double Blind Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
August 2013 (Actual)
Primary Completion Date
June 2015 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Xijing Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Prolonged periods of cardiopulmonary bypass (CPB) cause high levels of plasma free haemoglobin(Hb) and are associated with increased morbidity. We hypothesized that repletion of nitric oxide (NO) during and after the surgical procedure on CPB may protect against endothelium dysfunction and organ failure caused by plasma-Hb induced NO scavenging.
Detailed Description
Prolonged periods of cardiopulmonary bypass (CPB) cause high levels of plasma free haemoglobin(Hb) and are associated with increased morbidity. We hypothesized that repletion of nitric oxide (NO) during and after the surgical procedure on CPB may protect against endothelium dysfunction and organ failure caused by plasma-Hb induced NO scavenging. There are three possible beneficial mechanisms of delivering NO: Nitric oxide reduces ischemia-reperfusion injury (such as in acute myocardial infarction, stroke, and acute tubular necrosis). Nitric oxide has anti-inflammatory properties. As antioxidants, exogenous NO may reduce injury by counteracting the cytotoxic effects of reactive oxygen species, modulating leukocyte recruitment, edema formation and tissue disruption. Exogenous nitric oxide prevents noxious effects of hemolysis-associated NO dysregulation. During hemolysis, nitric oxide gas oxidized of plasma oxyhemoglobin to methemoglobin, thereby inhibiting endogenous endothelium NO scavenging by cell-free Hb. NO depletion during hemolysis and its sequelae. The release of plasma free Hb (with Fe2+ iron) by hemolysis avidly scavenges nitric oxide (NO) by the dioxygenation reaction. Elevated plasma ferrous Hb levels can induce a "NO deficiency" state. Reduced vascular nitric oxide levels can contribute to vasoconstriction, inflammation, and thrombosis, potentially contributing to systemic endothelial dysfunction after cardiac surgery with CPB.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Valve Diseases, Heart; Complications, Valve, Prosthesis, Cardiac Valve Replacement Complication

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
217 (Actual)

8. Arms, Groups, and Interventions

Arm Title
inhaled nitrogen
Arm Type
Placebo Comparator
Arm Description
Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, pure nitrogen (placebo) is mixed with pure O2 or air. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the NO is delivered through the inspiratory limb of the anesthetic or ventilator circuit.
Arm Title
inhaled nitric oxide
Arm Type
Experimental
Arm Description
Using an Inovent (Ikaria Inc, N.J., USA) or volumetrically-calibrated flowmeters, 800 ppm NO gas is mixed with pure O2 or air to obtain a final concentration of 80 ppm NO. During CPB the gas mixture is delivered through the extracorporeal oxygenator, after CPB the gas is delivered through the inspiratory limb of the anesthetic or ventilator circuit. NO, NO2 and O2 and methemoglobin levels are monitored by an unblinded observer.
Intervention Type
Other
Intervention Name(s)
inhaled nitric oxide
Intervention Description
Nitric oxide administration will commence at the onset of CPB and last for 24 hours. At the end of 24 hours, inhaled NO will be weaned and discontinued while carefully monitoring hemodynamics for a period of 2-4 hours.
Intervention Type
Other
Intervention Name(s)
inhaled Nitrogen
Intervention Description
Standard gas including nitrogen (the vehicle of the Nitric oxide) administration will commence at the onset of CPB and last for 24 hours. At the end of 24 hours, inhaled gases will be weaned and discontinued while carefully monitoring hemodynamics for a period of 2-4 hours.
Primary Outcome Measure Information:
Title
acute kidney injury
Description
acute kidney injury was defined by the KDIGO criteria
Time Frame
an increase of serum creatinine by 50% within 7 days after surgery, or an increase of serum creatinine by 0.3 mg/dl within 2 days after surgery
Secondary Outcome Measure Information:
Title
Chronic kidney disease
Description
defined as eGFR<60 mL/min/1.73m2
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
Loss of 25% of eGFR compared to baseline
Description
Loss of 25% of eGFR compared to baseline
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
Major adverse kidney events (MAKE)
Description
a composite outcome of loss of 25% of eGFR from baseline, end stage renal disease requiring a continuous renal replacement therapy and mortality.
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
Renal Replacement Therapy
Description
the incidence of need for Renal Replacement Therapy
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
Incidence of nonfatal stroke and nonfatal myocardial infarction.
Description
Nonfatal stroke will be assessed by the NIH Stroke Scale at baseline before surgery and at 28 days, 60 days, 90 days and 1 year after surgery. Nonfatal myocardial infarction is defined by the third universal definition of MI released in 2012 by the ESC/ACCF/AHA/WHF.
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
Quality of life
Description
The quality of life will be evaluated by the Katz Index of In dependence in Activities of Daily living
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Title
overall mortality
Description
all cause mortality
Time Frame
at 30 days, 90 days, and 1 year following ICU admission
Other Pre-specified Outcome Measures:
Title
In-hospital stay
Description
It is the length of hospital stay
Time Frame
Normally within 30 days, when patients was discharged from ICU
Title
ICU-stay
Description
It is the length of stay in ICU
Time Frame
Normally within 30 days, when patients was discharged from ICU
Title
Incidence of prolonged ventilation
Description
Prolonged ventilation is defined as patients remaining on the ventilator for more than 48 hours
Time Frame
During hospital stay, normally within 30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provide written informed consent Are > 18 years of age Elective cardiac or aortic surgery with CPB, when the surgeon plans double valve replacement. Stable pre-operative renal function, without dialysis. Exclusion Criteria: Emergent cardiac surgery Life expectancy < 1 year Hemodynamic instability as defined by a systolic blood pressure <90 mmHg Administration of ≥1 Packed Red Blood Cell transfusion in the week before surgery X-ray contrast infusion less than 1 week before surgery Anticipate administration of nephrotoxic agents, such as hydroxyethyl starch Evidence of intravascular or extravascular hemolysis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
lize Xiong, M.D.,Ph.D.
Organizational Affiliation
Xijing Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Xijing Hospital
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710032
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
33481401
Citation
Hu J, Rezoagli E, Zadek F, Bittner EA, Lei C, Berra L. Free Hemoglobin Ratio as a Novel Biomarker of Acute Kidney Injury After On-Pump Cardiac Surgery: Secondary Analysis of a Randomized Controlled Trial. Anesth Analg. 2021 Jun 1;132(6):1548-1558. doi: 10.1213/ANE.0000000000005381.
Results Reference
derived
PubMed Identifier
29932345
Citation
Lei C, Berra L, Rezoagli E, Yu B, Dong H, Yu S, Hou L, Chen M, Chen W, Wang H, Zheng Q, Shen J, Jin Z, Chen T, Zhao R, Christie E, Sabbisetti VS, Nordio F, Bonventre JV, Xiong L, Zapol WM. Nitric Oxide Decreases Acute Kidney Injury and Stage 3 Chronic Kidney Disease after Cardiac Surgery. Am J Respir Crit Care Med. 2018 Nov 15;198(10):1279-1287. doi: 10.1164/rccm.201710-2150OC.
Results Reference
derived

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Prevention of Renal Failure by Nitric Oxide in Prolonged Cardiopulmonary Bypass.

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