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| Sponsor: | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Collaborator: |
Pediatric Heart Network |
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00113087 |
Purpose
This study will evaluate the efficacy and safety of administering an angiotensin converting enzyme inhibitor (ACE-I) (enalapril) to infants with a functional single ventricle. The study will also compare the effect of ACE-I therapy to placebo on somatic growth and compare the effect of ACE-I therapy to placebo on signs and symptoms of heart failure, neurodevelopmental and functional status, ventricular geometry, function, and atrioventricular (AV) valve regurgitation. In addition, the study will determine the relationship between genetic polymorphisms linked to ventricular hypertrophy (enlarged heart) and the response to ACE-I therapy and compare the incidence of adverse events in subjects treated with ACE-I with those in subjects treated with placebo.
| Condition | Intervention | Phase |
|---|---|---|
|
Heart Defects, Congenital Heart Failure, Congestive |
Drug: Enalapril Drug: Placebo |
Phase III |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Trial of ACE Inhibition in Infants With Single Ventricle (A Trial Conducted by the Pediatric Heart Network) |
Neurodevelopmental status (PDI):
the Bayley Scales of Infant Development: Psychomotor Development index z-score .
| Enrollment: | 230 |
| Study Start Date: | August 2003 |
| Study Completion Date: | July 2008 |
| Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Enalapril
Enalapril (angiotensin converting enzyme inhibitor)
|
Drug: Enalapril
Enalapril to target dose of .4mg/kg/day divided to twice per day (BID)
Other Name: Enalapril
|
|
Placebo Comparator: Placebo
Placebo (Ora-Plus and Ora-Sweet)
|
Drug: Placebo
Participants will receive placebo
Other Name: placebo
|
BACKGROUND:
Growth impairment is common in infants and children with congenital heart disease, most often in the presence of congestive heart failure and/or cyanosis. Growth failure is noted in many infants with a single ventricle who manifest both cyanosis and heart failure that commonly persist after palliative surgery. Whether this impairment is related to persistent or progressive abnormalities in cardiac structure and function is not known. ACE-Is are widely used in the treatment of infants with severe congestive heart failure to improve cardiac function and somatic growth. The ability of an ACE-I to improve somatic growth in infants with a single ventricle has not been previously studied.
This study has been approved by the Institutional Review Boards/Research Ethics Boards of all participating clinical centers:
Hospital for Sick Children, Toronto, Canada
Children's Hospital Boston, Boston, MA
Columbia College of Physicians and Surgeons, New York, NY
Children's Hospital of Philadelphia, Philadelphia, PA
Duke University Medical Center, Durham, NC
Brody School of Medicine at East Carolina University, Greenville, NC
Wake Forest Baptist Medical Center, Winston Salem, NC
Medical University of South Carolina, Charleston, SC
Primary Children's Medical Center, Salt Lake City, UT
Children's Hospital of Wisconsin, Milwaukee, WI
Cincinnati Children's Hospital Medical Center, Cincinnati, OH
DESIGN NARRATIVE:
This is a prospective, randomized, double-blind, placebo-controlled trial of ACE-I in infants with a single ventricle. After stratification by ventricular anatomy, neonates will be randomly assigned to receive enalapril or placebo and then followed for 14 months.
Eligibility| Ages Eligible for Study: | up to 45 Days |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Massachusetts | |
| Children's Hospital Boston | |
| Boston, Massachusetts, United States, 02115 | |
| United States, New York | |
| Columbia College of Physicians and Surgeons | |
| New York, New York, United States, 10032 | |
| United States, North Carolina | |
| Duke University Medical Center | |
| Durham, North Carolina, United States, 27710 | |
| United States, Ohio | |
| Cincinnati Children's Hospital Medical Center | |
| Cincinnati, Ohio, United States, 45229 | |
| United States, Pennsylvania | |
| Children's Hospital of Philadelphia | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| United States, South Carolina | |
| Medical University of South Carolina | |
| Charleston, South Carolina, United States, 29425 | |
| United States, Utah | |
| Primary Children's Hospital | |
| Salt Lake City, Utah, United States, 84113 | |
| United States, Wisconsin | |
| Children's Hospital of Wisconsin | |
| Milwaukee, Wisconsin, United States, 53226 | |
| Canada, Ontario | |
| Hospital for Sick Children | |
| Toronto, Ontario, Canada, M5G 1X8 | |
| Principal Investigator: | Page Anderson, MD | Duke University Medical Center, Durham, NC |
| Principal Investigator: | Daphne Hsu, MD | The Children's Hospital at Montefiore, NYC, NY |
| Principal Investigator: | Brian McCrindle, MD | The Hospital for Sick Children |
| Principal Investigator: | LuAnn Minich, MD | Primary Children's Hospital, Salt Lake City, UT |
| Principal Investigator: | Jane Newburger, MD | Children's Hospital Boston, Boston, MA |
| Principal Investigator: | J. Philip Saul, MD | Medical University of South Carolina, Charleston, SC |
| Principal Investigator: | Lynn Sleeper, Sc.D. | New England Research Institute, Watertown, MA |
| Principal Investigator: | Victoria Vetter, MD | Children's Hospital of Philadelphia, Philadelphia, PA |
| Principal Investigator: | Woodrow Benson, MD | Cincinnati Children's Medical Center, Cincinnati, OH |
More Information
| Responsible Party: | Lynn Sleeper, PI, New England Research Institutes |
| ClinicalTrials.gov Identifier: | NCT00113087 History of Changes |
| Other Study ID Numbers: | 177, U01HL068270, U01HL068279, U01HL068281, U01HL068285, U01HL068288, U01HL068290, U01HL068292, U01HL068269 |
| Study First Received: | June 3, 2005 |
| Results First Received: | September 4, 2009 |
| Last Updated: | September 16, 2010 |
| Health Authority: | United States: Food and Drug Administration |
|
Congenital Abnormalities Heart Defects, Congenital Heart Failure Cardiovascular Abnormalities Cardiovascular Diseases Heart Diseases Angiotensin-Converting Enzyme Inhibitors Enalapril |
Enalaprilat Protease Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Pharmacologic Actions Antihypertensive Agents Cardiovascular Agents Therapeutic Uses |