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Tracking Information | |||||
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First Received Date † | December 20, 2005 | ||||
Last Updated Date | May 3, 2007 | ||||
Start Date † | June 2002 | ||||
Current Primary Outcome Measures † | |||||
Original Primary Outcome Measures † | |||||
Change History | Complete list of historical versions of study NCT00268034 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures † | |||||
Original Secondary Outcome Measures † | |||||
Descriptive Information | |||||
Brief Title † | Left Ventricular Aneurysms in Children | ||||
Official Title † | Left Ventricular Aneurysms in Children | ||||
Brief Summary | Collect data to support “standard of care possibility” of extracardiac repair with closure of intracavitary communication and plication of the aneurysm as probably safest surgical repair for left ventricular aneurysms. |
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Detailed Description | Ventricular aneurysms in the pediatric population are rare and no standardized method of treatment exists. We plan on reviewing five patient charts between the dates of 6.30.02 and 6.30.04 as to causes of aneurysms. The patient charts selected will be in the following “aneurysm categories”: Mostly occur after: Ross/Ross-Konno procedures modified Rastelli-type interventricular tunnels repeated resections of subaortic stenosis and possibly after: myocardial ischemia trauma drainage of abscess in infective endocarditis progressive herniation of endocardium mostly located: in LV outflow tract We plan on collecting echocardiograms and / or cardiac catheterizations data in order to confirm the diagnosis of an aneurysm. We will also collect the following information:
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Study Phase | |||||
Study Type † | Observational | ||||
Study Design † | Natural History, Longitudinal, Defined Population, Retrospective Study | ||||
Condition † | Congenital Disorders | ||||
Intervention † | |||||
Study Arms / Comparison Groups | |||||
Publications * | |||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||
Recruitment Status † | Terminated | ||||
Enrollment † | 5 | ||||
Completion Date | |||||
Primary Completion Date | |||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | up to 21 Years | ||||
Accepts Healthy Volunteers | No | ||||
Contacts †† | |||||
Location Countries † | United States | ||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00268034 | ||||
Responsible Party | |||||
Secondary IDs †† | |||||
Study Sponsor † | Children's Healthcare of Atlanta | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | Children's Healthcare of Atlanta | ||||
Verification Date | May 2007 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |