The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution
Primary Purpose
Hypertension, Congestive Cardiomyopathy
Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Enalaprilat
Sponsored by
About this trial
This is an interventional treatment trial for Hypertension focused on measuring pediatric, hypertension, congestive cardiomyopathy, angiotensin-converting enzyme inhibitor, cardiac catheterization
Eligibility Criteria
Inclusion Criteria:
- BCPC patients at time of routine pre-Fontan catheterization
- Patients between the ages of 2 months and 5 years old
Exclusion Criteria:
- Patients who have had ACEI therapy within 24 hours of the procedure
Sites / Locations
- The Hospital for Sick Children
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Enalaprilat
Arm Description
enalaprilat 0.005-0.01 mg/kg intravenous x 1 dose
Outcomes
Primary Outcome Measures
Systemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat
Systemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat
Systemic, pulmonary and cerebral resistance is compared at baseline and after enalaprilat
Secondary Outcome Measures
Full Information
NCT ID
NCT00741156
First Posted
August 25, 2008
Last Updated
November 16, 2015
Sponsor
The Hospital for Sick Children
1. Study Identification
Unique Protocol Identification Number
NCT00741156
Brief Title
The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution
Official Title
The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution After the Bidirectional Cavopulmonary Connection
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
July 2008 (undefined)
Primary Completion Date
January 2010 (Actual)
Study Completion Date
January 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The primary objective of this study is to study the acute effects of angiotensin-converting enzyme inhibitor (ACEI) on systemic, pulmonary and cerebral blood flow in post bidirectional cavopulmonary connection (BCPC) patients.
Detailed Description
The intermediate stage of the bi-directional cavopulmonary connection (BCPC) in the management algorithm of single ventricle palliation is a unique and extraordinary physiologic condition. It places the superior vena caval blood flow into series with the lungs i.e. pulmonary blood flow is partially dependent on cerebral vascular flow and resistance. Differential reduction in the resistances of the systemic, cerebral and pulmonary vascular beds will result in re-equilibrium of relative blood flows which translate to alterations in arterial oxygen tension and perfusion pressure. This concept is demonstrated by the differential effects of carbon dioxide (CO2) and oxygen (O2). CO2 vasodilates and oxygen (O2) vasoconstricts the cerebral vascular bed; the opposite is true in the lungs. Furthermore, studies have demonstrated that arterial CO2 tension (PaCO2) at hypercarbic levels is favourable to normocarbia in increasing pulmonary, systemic and cerebral blood flows and reducing systemic vascular resistance in acute post BCPC patients.
Administration of angiotensin-converting enzyme inhibitor (ACEI) and other systemic vasodilator drugs are well established for treatment of patients with hypertension and congestive cardiomyopathy in both pediatric and adult populations. Favourable manipulation of the flow to the different vascular beds has been reported in children with significant intra-cardiac shunts in which pulmonary blood flow is decreased relative to the increase in systemic blood flow as a result of reduction of systemic vascular resistance.
Guided by similar principles, ACEI therapy is administered to patients with single ventricle physiology to redistribute relative blood flows across the pulmonary and systemic vascular beds. To date, there exists no study examining the hemodynamic effects of ACEI on relative blood flows in the setting of single ventricle physiology and in particular, no study demonstrates its benefits. The effects of ACEI are unknown on the equilibrium of relative cerebral, systemic and pulmonary blood flows in the post-BCPC state. A relative increase in systemic blood flow, as effected by ACEI, at the expense of cerebral blood flow may potentially adversely decrease pulmonary blood and ultimately reduce arterial oxygen tension. On the other hand, some data suggests that ACEI's improve cerebral autoregulation function; in which drop in blood pressure will signal a vasodilatory response in the cerebral vascular bed which may be particularly advantageous in BCPC patients.
Enalaprilat is the active diacid of the ACEI enalapril maleate. Doses of 0.01 to 0.06 mg/kg i.v. have been safely administered in pediatric studies. Onset of action is 15 minutes and duration of action is up to 12-24 hours. The pharmacokinetics of this drug are ideal for the purpose of this study. In our institution, all patients undergo routine cardiac catheterization after the BCPC procedure for hemodynamic assessment and angiography of cardiac structures to assess for eligibility for the Fontan operation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Congestive Cardiomyopathy
Keywords
pediatric, hypertension, congestive cardiomyopathy, angiotensin-converting enzyme inhibitor, cardiac catheterization
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Enalaprilat
Arm Type
Experimental
Arm Description
enalaprilat 0.005-0.01 mg/kg intravenous x 1 dose
Intervention Type
Drug
Intervention Name(s)
Enalaprilat
Other Intervention Name(s)
Vasotec
Intervention Description
Enalaprilat will be administered intravenously i.v. 0.005 - 0.01 mg/kg i.v. over 1 minute
Primary Outcome Measure Information:
Title
Systemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat
Time Frame
Baseline and after enalaprilat
Title
Systemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat
Description
Systemic, pulmonary and cerebral resistance is compared at baseline and after enalaprilat
Time Frame
Baseline and after enalaprilat
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
BCPC patients at time of routine pre-Fontan catheterization
Patients between the ages of 2 months and 5 years old
Exclusion Criteria:
Patients who have had ACEI therapy within 24 hours of the procedure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kyong-Jin Lee, MD
Organizational Affiliation
The Hospital for Sick Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution
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