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Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass

Primary Purpose

Ischemia/Reperfusion Injury After Neonatal Cardiac Surgery, Inflammatory Reaction After Neonatal Cardiac Surgery

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Inhaled Nitric Oxide
placebo
Sponsored by
Chawki Elzein
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemia/Reperfusion Injury After Neonatal Cardiac Surgery focused on measuring Ischemia/reperfusion injury

Eligibility Criteria

1 Day - 30 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Neonates, age 0-30 days
  • Full term, > 37 weeks gestation
  • Birth weight ≥ 2.6 kg

Exclusion Criteria:

  • Preoperative sepsis
  • Preoperative renal dysfunction
  • Preoperative intracranial hemorrhage
  • Chromosomal abnormalities and/or genetic syndromes
  • Prior intervention (catheter based or surgical)

Sites / Locations

  • Advocate Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Nitric oxide on CPB

control

Arm Description

neonates receiving inhaled NO into the cardiopulmonary bypass circuit during cardiac surgery

neonates not receiving inhaled NO into the cardiopulmonary bypass

Outcomes

Primary Outcome Measures

Change in Biochemical Markers of Ischemia/Reperfusion Injury and Oxidative Damage (Positive ~ Increase From Pre-op)
The primary study endpoints are to evaluate whether NO delivered through the neonatal cardiopulmonary bypass (CPB) circuit can decrease various biochemical markers of ischemia/reperfusion injury and oxidative damage. Markers to be analyzed will include cardiac troponin I, interleukins (IL), tumor necrosis factor, N-terminal prohormone for brain natriuretic peptide (NT-proBNP),lactate dehydrogenase (LDH), plasma anti-oxidant levels, plasma malondialdehyde (MDA) levels.

Secondary Outcome Measures

Total Fluid Balance at 48 Hours
The secondary study endpoints are to evaluate whether NO delivered through the neonatal CPB circuit can decrease the clinical signs of ischemia/reperfusion injury and/or cardiac dysfunction. Clinical parameters (post surgery) include inotropic support, fluid balances, diuretic support, ventilator times, and length of ICU stay will be evaluated.
Time Until Start of Diuretic Therapy
hours until start of diuretic therapy
Inotropic Score Day 1
The Inotropic Score is an objective clinical tool used to quantify the need for cardiovascular support in children and adolescents after surgery and to predict prognosis of pediatric septic shock (higher score predicts higher risk or worse prognosis).The Inotropic Score is low if <= 20, intermediate if 21-30, and high if > 30. Formula used in the study: Daily inotropic score (mcg/kg/min) = Dopamine drip dose+ dobutamine drip dose+ (milrinone drip dose times 10) + (epinephrine drip dose times 100 )
Length of Intubation and PSHU Stay
Days to extubation and Pediatric Surgical Heart Unit (PSHU) length of stay (LOS) as measuring patient surgical outcomes.

Full Information

First Posted
May 27, 2014
Last Updated
April 2, 2020
Sponsor
Chawki Elzein
Collaborators
Mallinckrodt
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1. Study Identification

Unique Protocol Identification Number
NCT02151877
Brief Title
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass
Official Title
Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
August 15, 2018 (Actual)
Study Completion Date
August 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Chawki Elzein
Collaborators
Mallinckrodt

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Around 7500 neonates born yearly in the United States have complex congenital heart disease that require surgical repair in the first few days of life. The complexity of the surgical repair requires long periods of cardiopulmonary bypass (CPB) and the use of intermittent periods of low flow or complete circulatory arrest. The immature neonatal vital organs are more prone to the complications of the cardiopulmonary bypass circulation, namely ischemia/reperfusion (I/R) injury and systemic inflammatory response. Inhaled nitric oxide (NO) is used frequently in neonates for the treatment of pulmonary hypertension, Additionally, many studies have shown that NO has an anti-inflammatory effect by reducing I/R injury and endothelial dysfunction. The purpose of this pilot study is to assess the efficacy of NO administration via the CPB circuit in attenuating the CPB induced I/R injury and systemic inflammatory reaction in neonates undergoing repair of complex congenital heart defects. Specific goals will be to demonstrate that NO use via CPB will: Decrease markers of I/R injury and systemic inflammatory response. Decrease platelet activation leading to reduced postoperative bleeding and transfusion requirements. Decrease postoperative organ dysfunction, and hence decrease operative mortality and postoperative morbidity. Twelve neonates undergoing repair of complex congenital heart defects will receive NO via the CPB circuit, for the duration of surgery. They will be compared to a control group of 12 similar patients. Serum levels of different ischemic reperfusion injury and inflammatory markers will be measured at different time points after surgery and will be correlated with different end organ function tests and clinical course in the postoperative period. The results will be compared between the two groups to try to determine the clinical benefit of NO administration through CPB circuit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemia/Reperfusion Injury After Neonatal Cardiac Surgery, Inflammatory Reaction After Neonatal Cardiac Surgery
Keywords
Ischemia/reperfusion injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nitric oxide on CPB
Arm Type
Experimental
Arm Description
neonates receiving inhaled NO into the cardiopulmonary bypass circuit during cardiac surgery
Arm Title
control
Arm Type
Placebo Comparator
Arm Description
neonates not receiving inhaled NO into the cardiopulmonary bypass
Intervention Type
Drug
Intervention Name(s)
Inhaled Nitric Oxide
Other Intervention Name(s)
study group
Intervention Description
delivering inhaled Nitric Oxide into the cardiopulmonary bypass circuit during neonatal cardiac surgery
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
control group
Intervention Description
inhaled Nitric Oxide not delivered to the cardiopulmonary bypass circuit during neonatal cardiac surgery
Primary Outcome Measure Information:
Title
Change in Biochemical Markers of Ischemia/Reperfusion Injury and Oxidative Damage (Positive ~ Increase From Pre-op)
Description
The primary study endpoints are to evaluate whether NO delivered through the neonatal cardiopulmonary bypass (CPB) circuit can decrease various biochemical markers of ischemia/reperfusion injury and oxidative damage. Markers to be analyzed will include cardiac troponin I, interleukins (IL), tumor necrosis factor, N-terminal prohormone for brain natriuretic peptide (NT-proBNP),lactate dehydrogenase (LDH), plasma anti-oxidant levels, plasma malondialdehyde (MDA) levels.
Time Frame
Pre-op baseline and up to 12 hours after surgery
Secondary Outcome Measure Information:
Title
Total Fluid Balance at 48 Hours
Description
The secondary study endpoints are to evaluate whether NO delivered through the neonatal CPB circuit can decrease the clinical signs of ischemia/reperfusion injury and/or cardiac dysfunction. Clinical parameters (post surgery) include inotropic support, fluid balances, diuretic support, ventilator times, and length of ICU stay will be evaluated.
Time Frame
48 hours post surgery
Title
Time Until Start of Diuretic Therapy
Description
hours until start of diuretic therapy
Time Frame
Pre-op to 72 hours post surgery
Title
Inotropic Score Day 1
Description
The Inotropic Score is an objective clinical tool used to quantify the need for cardiovascular support in children and adolescents after surgery and to predict prognosis of pediatric septic shock (higher score predicts higher risk or worse prognosis).The Inotropic Score is low if <= 20, intermediate if 21-30, and high if > 30. Formula used in the study: Daily inotropic score (mcg/kg/min) = Dopamine drip dose+ dobutamine drip dose+ (milrinone drip dose times 10) + (epinephrine drip dose times 100 )
Time Frame
24 hours post surgery
Title
Length of Intubation and PSHU Stay
Description
Days to extubation and Pediatric Surgical Heart Unit (PSHU) length of stay (LOS) as measuring patient surgical outcomes.
Time Frame
Surgery to discharge
Other Pre-specified Outcome Measures:
Title
Surgical Morbidity
Description
include all complications that may happen after cardiac surgery for the whole period of hospital stay, that is expected to be around 1 month. This include renal failure, prolonged intubation and ventilatory support, infections..
Time Frame
1 month after cardiac surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
30 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Neonates, age 0-30 days Full term, > 37 weeks gestation Birth weight ≥ 2.6 kg Exclusion Criteria: Preoperative sepsis Preoperative renal dysfunction Preoperative intracranial hemorrhage Chromosomal abnormalities and/or genetic syndromes Prior intervention (catheter based or surgical)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chawki F Elzein, MD
Organizational Affiliation
Advocate Healthcare
Official's Role
Principal Investigator
Facility Information:
Facility Name
Advocate Children's Hospital
City
Oak Lawn
State/Province
Illinois
ZIP/Postal Code
60453
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
http://www.advocatechildrenshospital.com
Description
Related Info

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Efficacy of Nitric Oxide Administration in Attenuating Ischemia/Reperfusion Injury During Neonatal Cardiopulmonary Bypass

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