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The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution

The Acute Effects of the Angiotensin-converting Enzyme Inhibitor Enalaprilat on Flow Distribution After the Bidirectional Cavopulmonary Connection

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00741156
Enrollment
12
Registered
2008-08-26
Start date
2008-07-31
Completion date
2010-01-31
Last updated
2015-12-18

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

Conditions

Hypertension, Congestive Cardiomyopathy

Keywords

pediatric, hypertension, congestive cardiomyopathy, angiotensin-converting enzyme inhibitor, cardiac catheterization

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.

Interventions

Enalaprilat will be administered intravenously i.v. 0.005 - 0.01 mg/kg i.v. over 1 minute

Sponsors

The Hospital for Sick Children
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
2 Months to 5 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Systemic, Pulmonary and Cerebral Blood Flow at Baseline and After EnalaprilatBaseline and after enalaprilat
Systemic, Pulmonary and Cerebral Resistance at Baseline and After EnalaprilatBaseline and after enalaprilatSystemic, pulmonary and cerebral resistance is compared at baseline and after enalaprilat

Countries

Canada

Participant flow

Participants by arm

ArmCount
Enalaprilat
Enalaprilat : Enalaprilat will be administered intravenously i.v. 0.01 mg/kg i.v. over 1 minute
12
Total12

Baseline characteristics

CharacteristicEnalaprilat
Age, Categorical
<=18 years
12 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
0 Participants
Age, Continuous2.3 years
STANDARD_DEVIATION 1
Region of Enrollment
Canada
12 participants
Sex: Female, Male
Female
NA Participants
Sex: Female, Male
Male
NA Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
0 / 12
serious
Total, serious adverse events
0 / 12

Outcome results

Primary

Systemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat

Time frame: Baseline and after enalaprilat

ArmMeasureValue (MEDIAN)
Systemic Blood Flow BaselineSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.4 l/min/m2
Systemic Blood Flow After EnalaprilatSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.8 l/min/m2
Pulmonary Blood Flow BaselineSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.9 l/min/m2
Pulmonary Blood Flow After EnaliprilatSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.9 l/min/m2
Cerebral Blood Flow BaselineSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.9 l/min/m2
Cerebral Blood Flow After EnalaprilatSystemic, Pulmonary and Cerebral Blood Flow at Baseline and After Enalaprilat1.8 l/min/m2
p-value: 0.09Wilcoxon (Mann-Whitney)
Primary

Systemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat

Systemic, pulmonary and cerebral resistance is compared at baseline and after enalaprilat

Time frame: Baseline and after enalaprilat

ArmMeasureValue (MEDIAN)
Systemic Blood Flow BaselineSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat40.94 Wood units per metre squared
Systemic Blood Flow After EnalaprilatSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat20.26 Wood units per metre squared
Pulmonary Blood Flow BaselineSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat2.87 Wood units per metre squared
Pulmonary Blood Flow After EnaliprilatSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat2.54 Wood units per metre squared
Cerebral Blood Flow BaselineSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat24.07 Wood units per metre squared
Cerebral Blood Flow After EnalaprilatSystemic, Pulmonary and Cerebral Resistance at Baseline and After Enalaprilat17.32 Wood units per metre squared

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