Viewing Study NCT00315263



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Study NCT ID: NCT00315263
Status: COMPLETED
Last Update Posted: 2011-08-26
First Post: 2006-04-14

Brief Title: Genomics Single Nucleotide Polymorphisms SNPs and Clinical Neonatology
Sponsor: Childrens Mercy Hospital Kansas City
Organization: Childrens Mercy Hospital Kansas City

Study Overview

Official Title: Genomics SNPs and Clinical Neonatology
Status: COMPLETED
Status Verified Date: 2011-08
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: This research seeks to establish a neonatal DNA Tissue Bank to find out if differences in small segments of DNA predispose babies to Chronic Lung Disease CLD Periventricular Brain Injury PVI Necrotizing Enterocolitis NEC or Hypoxic Respiratory Failure HRF
Detailed Description: This genetic predisposition study does not involve investigational drugs devices or treatments Our broad goal is to identify genomic factors which contribute to the development or exacerbation of common and critical illnesses that affect preterm and near-term infants We seek to accomplish this goal in the following ways

First to test candidate gene DNA variations and link already identified single nucleotide polymorphisms SNPs producing functional alterations to the risk of clinically important disorders
Second to utilize a whole-genomic approach to identify SNPs not previously linked to the risk of development or progression of neonatal disorders

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