Clinical Trials Directory

Trials / Completed

CompletedNCT00383318

Demographic, Metabolic, and Genomic Description of Neonates With Severe Hyperbilirubinemia

Status
Completed
Phase
Study type
Observational
Enrollment
450 (estimated)
Sponsor
Pediatrix · Academic / Other
Sex
All
Age
6 Days
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the demographic, metabolic, and genomic characteristics of patients who develop severe hyperbilirubinemia to patients who never developed a significant bilirubin level.

Detailed description

The purpose of this study is to compare the demographic, metabolic, and genomic characteristics of patients who develop severe hyperbilirubinemia (serum bilirubin level in the "high risk zone of greater than the 95th percentile based on the Bhutani nomogram) to patients who never developed significant hyperbilirubinemia (bilirubin level in "low risk zone of less than the 40th percentile" on Bhutani nomogram and who did not require any treatment for hyperbilirubinemia). Our primary goal is to determine if common gene mutations occur at a greater frequency in patients with severe hyperbilirubinemia than in neonates without significant hyperbilirubinemia. The gene mutations we will test for are: * Glucose-6-phosphate Dehydrogenase Deficiency \[G6PD\] gene mutations * African A- mutation (G202A;A376G) * The common Mediterranean mutation (C563T) * Two common Chinese mutations (G1376T and G1388A) * UGT1A1 polymorphism. The UGT1A1 gene polymorphisms refer to those genetic defects found to be associated with Gilbert's Syndrome, including a promoter defect (T-3263G) that disrupts a transcription regulatory site, the TA repeats promoter polymorphism, and four mutations within the coding region (G211A, C686A, C1091T, and T1456G). * Gene polymorphism for the organic anion transporting protein (OATP-2)

Conditions

Interventions

TypeNameDescription
PROCEDUREGene mutation sample

Timeline

Start date
2006-09-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2006-10-03
Last updated
2008-01-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00383318. Inclusion in this directory is not an endorsement.