Preventing Acute Kidney Injury (AKI) in Pediatric Patients (AKI)
Primary Purpose
Acute Kidney Injury
Status
Recruiting
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Aminophylline
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Acute Kidney Injury focused on measuring Aminophylline
Eligibility Criteria
Inclusion Criteria:
Cohort 1
- All children undergoing open heart surgery for congenital heart defects with or without circulatory arrest
- Neonates (<28 days old) and infants (<1 years of age)
- Hypoplastic L heart syndrome or its variants.
- Coarctation with aortic arch hypoplasia.
- Interrupted aortic arch.
- TAPVR (Total anomalous pulmonary venous return)
- Patients with complex congenital heart defects
Cohort 2:
- Orthotopic heart transplantation patients.
- Patients ≤ 18 years of age
- Congenital heart defects
- Cardiomyopathy (Dilated/Hypertrophic/Restrictive/Left Ventricular Non-compaction)
Exclusion Criteria:
- Children under the age of 12 months undergoing bypass for any condition that is not categorized as congenital heart defect
- History of seizures
- History of significant tachyarrhythmia.
Sites / Locations
- LeBonheur Children's HospitalRecruiting
- LeBonheur Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Aminophylline pre CPB & immediately post CPB
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Acute kidney injury state II/III by AKIN criteria
Acute kidney injury state II/III by AKIN criteria
Secondary Outcome Measures
Urine output during post op
Urine output during post op
Urine output during post op
Urine output during post op
Concentration of Delta serum cystatin C
Delta serum cystatin C
Acute kidney injury stage
Acute kidney injury stage Pediatric modified Acute Kidney Injury Network criteria (pAKIN) AKI Stage I-<0.5mL (milliliter)/kg/hour for 8 hours AKI Stage II-<0.5mL/kg/hour for 16 hours AKI Stage III-<0.3mL/kg/hour for 24 hours OR Anuria for 16 hours
Using serum creatinine and AKIN criteria
Full Information
NCT ID
NCT03897335
First Posted
February 20, 2019
Last Updated
April 11, 2022
Sponsor
Le Bonheur Children's Hospital
1. Study Identification
Unique Protocol Identification Number
NCT03897335
Brief Title
Preventing Acute Kidney Injury (AKI) in Pediatric Patients
Acronym
AKI
Official Title
The Effect of Aminophylline on Preventing Acute Kidney Injury in Pediatric Patients Undergoing Open Heart Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
February 7, 2019 (Actual)
Primary Completion Date
February 1, 2023 (Anticipated)
Study Completion Date
February 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Le Bonheur Children's Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare the effects of peri-operative administration of Aminophylline versus Saline placebo in the preservation of renal function and the attenuation of renal injury in pediatric patients undergoing open heart surgery.
Detailed Description
Cardiac palliative/ correction surgeries in pediatric patients involve significant morbidity and mortality risks. Kidney function is frequently affected from cardiac surgery in these children. Studies identify the incidence of acute kidney injury (AKI) to be approximately 54% when defined by serum biomarkers (e.g. serum creatinine) and urine output criteria. The need for renal replacement therapy (RRT) for newborns and infants after cardiac surgery is reported as 2% to 17% in the literature. There are several reported risk factors for the development of AKI in this population. These are the complexities of the underlying heart disease and the surgical procedure, duration of cardiopulmonary bypass, functional single ventricle heart disease, circulatory arrest and low cardiac output syndrome in the post-operative period. AKI can cause worsening fluid overload compromising ventilation and lung function, predisposition to overwhelming infections and cytokine-mediated inflammatory state. The presence of AKI significantly increases the mortality that is associated with cardiac surgery in these very young patients, reported as high as 79% in the literature. There have been several reports suggesting that early intervention with AKI using renal replacement therapy (RRT) may improve patient mortality. Successful prevention strategies for AKI have not been reported for this high-risk population.
Adenosine has been demonstrated to regulate renal circulation and metabolism. It is a breakdown product of adenosine triphosphate/adenosine diphosphate (ATP/ADP) metabolism and accumulates in AKI. At baseline, the barely detectable renal parenchymal adenosine levels can increase to 10-100 times following an ischemic insult. These are typical seven trans-membrane spanning domains with a coupled G-protein at the intracellular end. Adenosine receptors are located ubiquitously in many tissues. Adenosine acts as a vasodilator in all other tissues but the renal parenchyma. The interaction of AT-II with adenosine converts adenosine to a vasoconstrictor in renal microvasculature. Adenosine acts on the A1 receptors (A1 R) in the afferent arterioles, causing reduced glomerular blood flow and glomerular filtration rate (GFR), as well as stimulating renin release from the kidney parenchyma. Adenosine plays an important role in generating the vasoconstrictive response in the renal vasculature to hypoxia and ischemia. Early interventions by blocking the actions of adenosine on A1 R may restore glomerular blood flow and recover GFR.
The study rationale is that Aminophylline and Theophylline are competitive non-selective inhibitors of adenosine. Therefore, even though aminophylline infusion (iv) has no effect on renal blood flow rate at baseline, it can ameliorate the decrease in renal blood flow rate following adenosine infusion. This property can improve renal function when the main mechanism of insult induces vasoconstriction. Both early and late administration of aminophylline protects renal function after ischemia-reperfusion injury in rats. Aminophylline has also been reported to successfully reverse newborn renal failure, prevent renal failure in perinatal asphyxia, and reverse acute kidney injury secondary to calcineurin induced nephropathy. Both theophylline and aminophylline have been used for prophylaxis of renal impairment during aorto-coronary bypass surgery in adults and the results have not been consistent for either a positive or negative effect. There have been no trials reported on the effect of aminophylline or theophylline to prevent or ameliorate acute kidney injury in children with congenital heart defects going through cardiac surgery.
Additionally, we are examining the components of serotonin biosynthesis to determine if these levels can act as markers of acute kidney injury in pediatric patients undergoing open heart surgery.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Kidney Injury
Keywords
Aminophylline
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
1 Patient randomization groups
A) Group 1: Aminophylline pre CPB & immediately post cardiopulmonary bypass (CPB)
B) Group 2: No aminophylline prophylaxis
Masking
ParticipantCare ProviderInvestigator
Masking Description
Cohort 1 will consist of all children undergoing open heart surgery for congenital heart defects with or without circulatory arrest, and Cohort 2 will consist of Orthotopic heart transplantation patients. All subjects will be randomized 1:1 to aminophylline or saline placebo. Cohort 1 will be randomized using block-stratification with stratification factors age (neonate vs infant) and circulatory arrest (yes vs no). Age will be categorized as neonates (0 to <28 days) and infants (28 days to <1 year).
A total of 80 (60 in Cohort 1 and 20 in Cohort 2) participants are expected to be enrolled on this study.
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Aminophylline pre CPB & immediately post CPB
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Aminophylline
Intervention Description
Aminophylline pre cardiopulmonary bypass and immediately post cardiopulmonary bypass. The dose will be Aminophylline 5 mg/kg/dose, max 350 mg slow infusion. The infusion rate duration will be standardized to 20 minutes. There will be no other aminophylline treatments for the first post-op five days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal Saline
Intervention Description
The placebo group will not receive any aminophylline treatments for the first post-op five days
Primary Outcome Measure Information:
Title
Acute kidney injury state II/III by AKIN criteria
Description
Acute kidney injury state II/III by AKIN criteria
Time Frame
At 48 hours post-operative
Secondary Outcome Measure Information:
Title
Urine output during post op
Description
Urine output during post op
Time Frame
first 12 hours post op
Title
Urine output during post op
Description
Urine output during post op
Time Frame
daily until 3 days post op
Title
Concentration of Delta serum cystatin C
Description
Delta serum cystatin C
Time Frame
24 hours post CPB
Title
Acute kidney injury stage
Description
Acute kidney injury stage Pediatric modified Acute Kidney Injury Network criteria (pAKIN) AKI Stage I-<0.5mL (milliliter)/kg/hour for 8 hours AKI Stage II-<0.5mL/kg/hour for 16 hours AKI Stage III-<0.3mL/kg/hour for 24 hours OR Anuria for 16 hours
Using serum creatinine and AKIN criteria
Time Frame
max point within post CPB 72 hours
Other Pre-specified Outcome Measures:
Title
Concentration of Delta urinary neutrophil gelatinase-associated lipocalin (NGAL)
Description
1 Delta urinary NGAL at 6 hours post cardiopulmonary (CPB) and Delta plasma NGAL at 2 hours post CPB.
Time Frame
at 2 hours post CPB.
Title
Time to extubation (hours)
Description
Time to extubation (hours) number of hours post surgery
Time Frame
during hospitalization, up to 8 days
Title
Time to chest closure (hours)
Description
Time to chest closure (hours) from start time of incision to chest closure during procedure
Time Frame
during hospitalization, up to 3 days
Title
Time to discharge from cardiovascular intensive care unit (CVICU) (days)
Description
Time to discharge from CVICU (days)
Time Frame
during hospitalization, approximate 5 days
Title
Duration of hospital stay (Days).
Description
Duration of hospital stay (Days).
Time Frame
during hospitalization, approximate 8 days
Title
Dialysis requirement (yes/no)
Description
Dialysis requirement (yes/no)
Time Frame
during hospitalization, approximate 5 days
Title
Time to return to preoperative weight.
Description
Time to return to preoperative weight.
Time Frame
during hospitalization, approximate 8 days
Title
Inotropic score
Description
Inotropic score Calculation of Inotropic score (IS) and Vasoactive inotropic score (VIS). IS(a) = dopamine dose (lg/kg/min) ? dobutamine dose (lg/kg/min) ? 100 9 epinephrine dose (lg/kg/min) VIS(b) = IS ? 10 9 milrinone dose (lg/kg/ min) ? 10,000 9 vasopressin dose (U/kg/ min) ? 100 9 norepinephrine dose (lg/kg/min) IS inotrope score, VIS vasoactive-inotropic score
Time Frame
at 7 days post operative
Title
Peritoneal dialysis catheter output.
Description
Peritoneal dialysis catheter output through study completion
Time Frame
during hospitalization, up to 8 days
Title
Transfusion requirements intraoperatively and postoperatively
Description
Transfusion requirements intraoperatively and postoperatively through study completion
Time Frame
during hospitalization, up to 8 days
Title
Inotropic score
Description
Inotropic score Calculation of Inotropic score (IS) and Vasoactive inotropic score (VIS). IS(a) = dopamine dose (lg/kg/min) ? dobutamine dose (lg/kg/min) ? 100 9 epinephrine dose (lg/kg/min) VIS(b) = IS ? 10 9 milrinone dose (lg/kg/ min) ? 10,000 9 vasopressin dose (U/kg/ min) ? 100 9 norepinephrine dose (lg/kg/min) IS inotrope score, VIS vasoactive-inotropic score
Time Frame
at 5 days post operative
10. Eligibility
Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Cohort 1
All children undergoing open heart surgery for congenital heart defects with or without circulatory arrest
Neonates (<28 days old) and infants (<1 years of age)
Hypoplastic L heart syndrome or its variants.
Coarctation with aortic arch hypoplasia.
Interrupted aortic arch.
TAPVR (Total anomalous pulmonary venous return)
Patients with complex congenital heart defects
Cohort 2:
Orthotopic heart transplantation patients.
Patients ≤ 18 years of age
Congenital heart defects
Cardiomyopathy (Dilated/Hypertrophic/Restrictive/Left Ventricular Non-compaction)
Exclusion Criteria:
Children under the age of 12 months undergoing bypass for any condition that is not categorized as congenital heart defect
History of seizures
History of significant tachyarrhythmia.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren Davis
Phone
901-287-4594
Email
lauren.davis2@lebonheur.org
First Name & Middle Initial & Last Name or Official Title & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org
Facility Information:
Facility Name
LeBonheur Children's Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lauren Davis
Phone
901-287-4594
Email
lauren.davis2@lebonheur.org
First Name & Middle Initial & Last Name & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org
Facility Name
LeBonheur Children's Hospital
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38103
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Umar S Boston, MD
Phone
901-287-5958
Email
uboston@uthsc.edu
First Name & Middle Initial & Last Name & Degree
Kerry Moore, RN
Phone
901-287-6871
Email
kerry.moore@lebonheur.org
12. IPD Sharing Statement
Plan to Share IPD
No
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Preventing Acute Kidney Injury (AKI) in Pediatric Patients
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