Genetic Susceptibility for Bronchopulmonary Dysplasia in Preterm Infants
NCT ID: NCT00904774
Last Updated: 2009-05-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
800 participants
OBSERVATIONAL
2009-05-31
Brief Summary
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1. a genome-wide association (GWA) study in VLBW neonates,
2. a candidate-gene association study, including selection of single nucleotide polymorphisms (SNPs) found in (a) and
3. functional studies of any SNP found to be convincingly associated with BPD in (a) and (b).
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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premature neonates
gestational age less than 28 weeks
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Inborn birth
* Prophylactic administration of surfactant in the delivery room
* Written informed consent obtained from parents
Exclusion Criteria
* Outborn birth
* No prophylactic administration of surfactant in the delivery room
* Congenital malformation
* Absence of written informed consent obtained from parents
8 Weeks
ALL
No
Sponsors
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Centre Hospitalier Intercommunal Creteil
OTHER
Responsible Party
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INSERM U955
Locations
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Centre Hospitalier Intercommunal
Créteil, , France
Countries
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References
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Hadchouel A, Decobert F, Franco-Montoya ML, Halphen I, Jarreau PH, Boucherat O, Martin E, Benachi A, Amselem S, Bourbon J, Danan C, Delacourt C. Matrix metalloproteinase gene polymorphisms and bronchopulmonary dysplasia: identification of MMP16 as a new player in lung development. PLoS One. 2008 Sep 11;3(9):e3188. doi: 10.1371/journal.pone.0003188.
Related Links
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The french PremUp Foundation is dedicated to pregnancy and the newborn
Other Identifiers
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AOR 07 018
Identifier Type: -
Identifier Source: org_study_id
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