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Nitric Oxide During Cardiopulmonary Bypass in Neonates to Reduce Risk of Acute Kidney Injury

Efficacy of Nitric Oxide Administration During Cardiopulmonary Bypass in Neonates at Reducing the Risk of Acute Kidney Injury: a Preliminary Double-blind Randomized Controlled Trial

Status
Withdrawn
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04259684
Enrollment
0
Registered
2020-02-06
Start date
2019-10-20
Completion date
2019-10-20
Last updated
2020-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Kidney Injury, Congenital Heart Disease

Brief summary

Acute kidney injury following cardiac surgery for congenital heart defects in children is a major cause of both short- and long-term morbidity and mortality, affecting up to 60% of high risk patients. Despite effort, to date, no successful therapeutic agent has gained widespread success in preventing this postoperative decline in renal function. Based on preliminary data available in the literature, we hypothesize that nitric oxide (gNO), administered during cardiopulmonary bypass (CPB), may reduce the risk of acute kidney injury (AKI) via mechanisms of reduced inflammation and vasodilation. In this pilot study, 40 neonates undergoing cardiac surgery will be randomized to receive intraoperative administration of 20 ppm of nitric oxide to the oxygenator of the cardiopulmonary bypass circuit or standard CPB with no additional gas.

Interventions

DRUGgases Nitric Oxide (gNO)

Participants in the intervention group will receive gNO blended into the fresh gas flow of the cardiopulmonary bypass (CPB) oxygenator and maintained at 20 ppm via an Ikaria INO Max DSIR (Mallinckrodt Pharmaceuticals, St. Louis, Missouri, USA), with continuous sampling of NO and NO2 concentration from a port adjacent to the oxygenator. The gNO delivery will be initiated when the patient is on CPB and stopped once the patient comes off CPB.

Sponsors

Children's Hospital Medical Center, Cincinnati
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

Each of the 40 participants will be stratified based on type of lesion (single ventricle vs. biventricular lesions) and block randomized into 1 of 2 study arms: treatment arm (receiving intraoperative administration of 20 ppm of gNO to the oxygenator of the CPB circuit) and control arm (standard CPB conduct).

Eligibility

Sex/Gender
ALL
Age
No minimum to 31 Days
Healthy volunteers
No

Inclusion criteria

* Neonates (≤31 days) undergoing cardiac surgery with cardiopulmonary bypass for congenital heart disease

Exclusion criteria

* 1\. Failure to obtain informed consent from parent/guardian, * Clinical signs of preoperative persistent elevated pulmonary vascular resistance, * Emergency surgery, * Episode of cardiac arrest within 1 week before surgery, * Recent treatment with steroids and/or a condition that may require treatment with steroids (excluding steroid administration specifically for CPB), * Use of inhaled NO (iNO) immediately prior to surgery, * Structural renal abnormalities by ultrasound, * Preoperative AKI, * Use of other investigational drugs, * Weight less than \<2.2 kg, * Gestational age \<36 weeks, * Major extracardiac congenital anomalies.

Design outcomes

Primary

MeasureTime frameDescription
Acute Kidney Injuryup to 72 hours postoperativeOccurrence of acute kidney defined by the Kidney Disease Improving Global Outcomes (KDIGO) diagnostic classification (employing both serum creatinine and urine output criteria).
Glomerular Filtration Rateup to 72 hours postoperativePostoperative glomerular filtration rate (GFR) measured using serum cystatin C.

Secondary

MeasureTime frameDescription
ECMO free daysup to 2 weeks after surgery to CICU dischargeExtracorporeal Membrane Oxygenation free days
Closed sternum daysup to 2 weeks from postoperative CICU admission to dischargedays
Structural Kidney Injuryup to 72 hours postoperativeAssessed by measurement of urine biomarkers: neutrophil gelatinase-associated lipocalin (NGAL), kidney injury molecule-1 (KIM-1), interleukin-18 (IL-18) liver-type fatty acid-binding protein (L-FABP), and urinary nitrate.
Low cardiac output syndrome (LCOS)up to 48 hours postoperativeOccurence of low cardiac output syndrome (LCOS) defined as any of the following at any time during the first 48 hours postoperative: 1. Lactate \>6mmol/l and central venous saturation (ScvO2) \<60% (or SaO2-ScvO2 difference greater than 35% in a single ventricle), 2. Vasoactive inotropic score (VIS)24 ≥ 10, 3. Extracorporeal Membrane Oxygenation (ECMO).
Duration of mechanical ventilationup to 2 weeks from admission to CICU to extubationhours/days
Time to negative fluid balanceup to 2 weeks from CICU admission to outcome reachedhours/days
Length of hospital stayup to 30 days from hospital admission to dischargedays
Urine Outputup to two weeks from CICU admission to dischargeml
Use of peritoneal dialysisup to two weeks from CICU admission to dischargeyes/no
Cardiac arrestup to two weeks from CICU admission to dischargeyes/no
Use of postoperative inhaled Nitric Oxide (iNO)up to two weeks from CICU admission to dischargeyes/no, indication, dose
Length of cardiac intensive care unit (CICU) stayup to 2 weeksfrom admission to CICU to discharge from CICUdays
Inotrope free daysup to 30 days after surgery to CICU dischargedays

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026