Neurological Fate, Prematurity and Genetic Susceptibility Factors

NCT04298346 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 27

Last updated 2023-08-04

No results posted yet for this study

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.

Conditions

  • Polymorphism, Restriction Fragment Length
  • Premature
  • Infertility of Cervical Origin

Interventions

OTHER

no intervention

no intervention

Sponsors & Collaborators

  • Nantes University Hospital

    lead OTHER

Eligibility

Min Age
5 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-03-09
Primary Completion
2022-03-09
Completion
2022-03-09

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04298346 on ClinicalTrials.gov