Viewing Study NCT00366561



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Study NCT ID: NCT00366561
Status: COMPLETED
Last Update Posted: 2014-12-02
First Post: 2006-08-17

Brief Title: Neonates With Neurological Complications
Sponsor: Childrens Healthcare of Atlanta
Organization: Childrens Healthcare of Atlanta

Study Overview

Official Title: Retrospective Review of Neonates With Neurological Complications Following Cardiac Surgery
Status: COMPLETED
Status Verified Date: 2014-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this retrospective study is to identify all neonates newborns 30 days of age from January 1 2002 through June 20 2006 at Childrens Healthcare of Atlanta who have suffered neurological complications following cardiac surgery This retrospective study is important to identify the incidence care and follow-up of neurological complications at this institution
Detailed Description: Studies have shown that between one-quarter and one-half of infants undergoing cardiac surgery will suffer brain injury during surgery the perioperative period Some infants with congenital heart disease have neurological injury prior to cardiac surgery as a result of cyanosis acidosis and abnormal circulation The spectrum of neurological injury ranges from agitation and subtle disturbances in learning and new memory acquisition to visual and motor development abnormalities seizures stroke and encephalopathy

The patient will be identified from the cardiothoracic surgery database Their hospital medical records and the neurological database will be reviewed for type of neurological complication ie seizure stroke neuro-imaging and any mortality for these patients We will review the patient outcome data that is available after the initial surgery through June 20 2006 No patients will be contacted

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None