Retrospective Evaluation of Carvedilol Versus Captopril in CHF Patients
Information source: Children's Healthcare of Atlanta
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Heart Failure; Heart Murmurs
Phase: N/A
Status: Terminated
Sponsored by: Children's Healthcare of Atlanta Official(s) and/or principal investigator(s): Jeffrey D Dayton, MD, Principal Investigator, Affiliation: Resident-Emory Department of Pediatrics
Summary
This is a retrospective chart review examining our experience with carvedilol in CHF
secondary to left-to-right heart shunt lesions. The treatment group will be children who
have received carvedilol. The control or comparison groups will be patients who have
received either digoxin/furosemide or captopril for this indication. Charts will be reviewed
of patients who have been treated at Children’s Healthcare of Atlanta and as outpatients by
Sibley Heart Center Cardiology between September 2000 and October 2005. Patients will have
been started on carvedilol prior to April 1, 2005 and only information up to October 1, 2005
will be used for this study. We will review approximately 50 charts for this study.
We will evaluate the effectiveness of these medications at reducing symptoms of CHF.
Clinical Details
Official title: The Retrospective Evaluation of Carvedilol Versus Captopril and Digoxin/Lasix Therapy in Congestive Heart Failure Due to Left-to-Right Shunt Lesions
Study design: Natural History, Longitudinal, Defined Population, Retrospective Study
Detailed description:
This is a retrospective chart review examining our experience with carvedilol in CHF
secondary to left-to-right heart shunt lesions. The treatment group will be children who
have received carvedilol. The control or comparison groups will be patients who have
received either digoxin/furosemide or captopril for this indication. Charts will be reviewed
of patients who have been treated at Children’s Healthcare of Atlanta and as outpatients by
Sibley Heart Center Cardiology between September 2000 and October 2005. Patients will have
been started on carvedilol prior to April 1, 2005 and only information up to October 1, 2005
will be used for this study. We will review approximately 50 charts for this study.
We will evaluate the effectiveness of these medications at reducing symptoms of CHF.
Eligibility
Minimum age: N/A.
Maximum age: 18 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria: Children aged 0-18 years with a cardiac defect resulting in a
left-to-right shunt (i. e. ventricular septal defect) who develop congestive heart failure.
Patient must have been treated with one of the study medications: carvedilol, digoxin, or
furosemide.
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Exclusion Criteria: Patients who are not between 0-18, who do not have a defect resulting
in left-to-right shunt, who do not have congestive heart failure and who have not been
treated with one of the study medications: carvedilol, digoxin, or furosemide.
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Locations and Contacts
Children's Healthcare of Atlanta, Atlanta, Georgia 30322, United States
Additional Information
Starting date: October 2005
Ending date: October 2005
Last updated: June 12, 2007
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