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Clinical Trial Summary

This study could help identify aggravating or protective genetic polymorphisms associated with cerebral palsy. Populations of premature babies at different risk of cerebral palsy could thus be individualized with an impact on their monitoring and on the pathophysiological understanding of the processes leading to neurological lesions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04298346
Study type Observational
Source Nantes University Hospital
Contact
Status Completed
Phase
Start date March 9, 2020
Completion date March 9, 2022

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