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NCT00014859 · ClinicalTrials.gov registry record

Epidemiology of Surfactant Protein-B Deficiency

A clinical trial, sponsored by Washington University School of Medicine.

Completed
Registry status
5,176
Enrollment target

NCT00014859: Completed study, sponsored by Washington University School of Medicine.

NCT00014859 is a clinical trial that has completed, run by Washington University School of Medicine. The registered enrollment target is 5,176 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00014859 has completed, sponsored by Washington University School of Medicine.

COMPLETED
Registry status
5,176 participants
Enrollment target

Study Summary

The purpose of this study is to test the hypothesis that excess, rare, functionally disruptive single nucleotide polymorphisms (SNPs) characterize genes (e.g., the surfactant protein-B gene)(SFTPB) and gene networks (e.g., the pulmonary surfactant metabolic network or other gene networks that regulate alveolar type 2 cell function) associated with increased risk of neonatal respiratory distress syndrome (RDS).

Primary Outcome

Using trio whole exome or whole genome sequencing, next generation sequencing, and in silico prediction of function, discover statistical associations between gene loci with excess, rare, functionally disruptive variants and risk of neonatal respiratory distress syndrome.

Trial Details

FieldValue
Enrollment Target 5,176 participants
Start Date 2001-06-01
Est. Completion 2024-04-26

What the finished NCT00014859 record still lists

NCT00014859 is an observational study that tracks outcomes without assigning an intervention. Its 5,176 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 0 interventions.

NCT00014859 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00014859 about?

NCT00014859 is a clinical study titled "Epidemiology of Surfactant Protein-B Deficiency". The purpose of this study is to test the hypothesis that excess, rare, functionally disruptive single nucleotide polymorphisms (SNPs) characterize genes (e.g., the surfactant protein-B gene)(SFTPB) and gene networks (e.g., the pulmonary surfactant metabolic network or other gene networks that regula...

What is the current status of trial NCT00014859?

This trial is currently completed. The enrollment target is 5,176 participants. The study started on 2001-06-01. Estimated completion is 2024-04-26.

Who is sponsoring clinical trial NCT00014859?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00014859, the US trial registry maintained by the National Library of Medicine. NCT00014859 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.