Preventing Brain Injury in Infants With Congenital Heart Disease
Primary Purpose
Cyanotic Congenital Heart Disease
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Topiramate
No medication, but routine heart surgery
Sponsored by
About this trial
This is an interventional prevention trial for Cyanotic Congenital Heart Disease focused on measuring brain injury, stroke, cerebral palsy, seizures
Eligibility Criteria
Inclusion Criteria:
- Age less than 2 months
- Cyanotic congenital heart disease requiring surgery
Exclusion Criteria:
- Genetic syndromes with high risk of neurodevelopmental delay
- Gestational age less than 35 weeks at birth
- Multiple organ failure or multiple organ anomalies
Sites / Locations
- UC Davis Children's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Topiramate
Control
Arm Description
These infants will undergo surgery, but will not receive topiramate
Outcomes
Primary Outcome Measures
Change from baseline in Plasma S100B
Baseline plasma S100B levels will be determined prior to surgery (at enrollment) with repeat levels at the two timepoints after surgery. Main outcome will be change from baseline.
Secondary Outcome Measures
Mullen Scales of Early Learning
This broad assessment of neurodevelopment includes five scales: Gross Motor, Visual Reception, Fine Motor, Expressive Language, and Receptive Language, with further testing if needed to explore deficits.
Changes from baseline in urine metabolomics
Urine specimens obtained at enrollment and at the two time points after surgery will be assessed for a broad range of metabolites (complex molecules). Changes from baseline will be evaluated.
Full Information
NCT ID
NCT01426542
First Posted
August 5, 2011
Last Updated
February 7, 2019
Sponsor
University of California, Davis
1. Study Identification
Unique Protocol Identification Number
NCT01426542
Brief Title
Preventing Brain Injury in Infants With Congenital Heart Disease
Official Title
Pilot Study of Topiramate Prophylaxis in Infants Undergoing Surgery for Congenital Heart Disease
Study Type
Interventional
2. Study Status
Record Verification Date
February 2019
Overall Recruitment Status
Completed
Study Start Date
March 2011 (undefined)
Primary Completion Date
July 28, 2017 (Actual)
Study Completion Date
July 28, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, Davis
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Newborn babies with congenital heart disease often require surgery in the first month of life. The risks of brain damage from congenital heart disease and from the various corrective surgeries are high because of poor levels of oxygen reaching the brain. Topiramate is an anti-convulsant medication that protects brain cells from damage due to low amounts of oxygen in animal studies. The investigators hypothesize that giving topiramate to babies with congenital heart disease before and after surgery will decrease the amount of brain damage caused by the heart disease and/or the surgery to correct the heart disease.
Detailed Description
Infants with cyanotic congenital heart disease undergoing surgery in the neonatal period have a high rate of brain injury resulting in seizures, stroke, cerebral palsy, and neurodevelopmental delays. Neuroimaging abnormalities are found in 30% to 60% of cases and neurodevelopmental impairments occur in more than half of these children. The mechanisms of brain injury in these children are not fully understood. Experimental animal models have shown that the abundant release of glutamate in the brain during hypoxic-ischemic insult results in brain injury. Blocking glutamate receptors by administration of the anticonvulsant topiramate has been shown to prevent such injury in animal studies. This study is an open pilot trial of peri-operative topiramate administration to infants with cyanotic congenital heart disease to test the feasibility of this approach and generate preliminary data about markers of brain injury (serum S100B levels and urine metabolomics) and neurodevelopment at 18 months of age. If the approach is feasible and the preliminary data are encouraging a larger efficacy trial will be designed. Although topiramate has been used in neonates and infants to treat seizures and in a pilot study in term infants with hypoxic-ischemic encephalopathy, this is the first study of its effects on markers of brain injury and neurologic outcomes in infants with cyanotic congenital heart disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cyanotic Congenital Heart Disease
Keywords
brain injury, stroke, cerebral palsy, seizures
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
24 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Topiramate
Arm Type
Experimental
Arm Title
Control
Arm Type
Active Comparator
Arm Description
These infants will undergo surgery, but will not receive topiramate
Intervention Type
Drug
Intervention Name(s)
Topiramate
Intervention Description
Topiramate 5 mg/kg by mouth (or by feeding tube) once a day for one week before and one week after heart surgery.
Intervention Type
Other
Intervention Name(s)
No medication, but routine heart surgery
Intervention Description
No medication, but routine heart surgery
Primary Outcome Measure Information:
Title
Change from baseline in Plasma S100B
Description
Baseline plasma S100B levels will be determined prior to surgery (at enrollment) with repeat levels at the two timepoints after surgery. Main outcome will be change from baseline.
Time Frame
1 week before surgery, 1 day and 1 week after surgery
Secondary Outcome Measure Information:
Title
Mullen Scales of Early Learning
Description
This broad assessment of neurodevelopment includes five scales: Gross Motor, Visual Reception, Fine Motor, Expressive Language, and Receptive Language, with further testing if needed to explore deficits.
Time Frame
18 months of age
Title
Changes from baseline in urine metabolomics
Description
Urine specimens obtained at enrollment and at the two time points after surgery will be assessed for a broad range of metabolites (complex molecules). Changes from baseline will be evaluated.
Time Frame
1 week before surgery, 1 day and 1 week after surgery
10. Eligibility
Sex
All
Maximum Age & Unit of Time
2 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age less than 2 months
Cyanotic congenital heart disease requiring surgery
Exclusion Criteria:
Genetic syndromes with high risk of neurodevelopmental delay
Gestational age less than 35 weeks at birth
Multiple organ failure or multiple organ anomalies
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark A Underwood, MD
Organizational Affiliation
University of California, Davis
Official's Role
Principal Investigator
Facility Information:
Facility Name
UC Davis Children's Hospital
City
Sacramento
State/Province
California
ZIP/Postal Code
95817
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Preventing Brain Injury in Infants With Congenital Heart Disease
We'll reach out to this number within 24 hrs