RecruitingNCT06244433

Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome


Sponsor

Nantes University Hospital

Enrollment

650 participants

Start Date

Aug 27, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

This is a multicenter genetic study aimed at identifying new genes/variants associated with sudden infant death syndrome (SIDS) based on whole-genome sequencing of family trios


Eligibility

Inclusion Criteria5

  • Death of a child between 0 and 2 years of age due to sudden unexpected death in infant
  • Child included in the French SUDI registry with effective participation in the biocollection
  • Biological parents of the child included in the BIOMINRISK study
  • Parents who have both signed the consent form for blood collection and inclusion of their samples in the biocollection
  • parents beneficiaries of a social security or similar scheme

Exclusion Criteria4

  • Presence of a known metabolic, genetic or syndromic pathology at the time of death
  • Parents Exclusion Crtiteria:
  • Parent under guardianship
  • Presence of a known metabolic, genetic or syndromic pathology

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Interventions

GENETICwhole genome sequencing

Study of all coding and non-coding sequences in the genome to identify pathogenic allelic variants


Locations(15)

Nantes University Hospital

Nantes, Loire-Atlantique, France

CHU Amiens

Amiens, France

CHU Angers

Angers, France

CHU Besançon

Besançon, France

APHP - Hôpital Jean Verdier

Bondy, France

CHU Brest

Brest, France

APHP - Hôpital Antoine Béclère

Clamart, France

CHU Grenoble

Grenoble, France

HCL

Lyon, France

AP-HM

Marseille, France

CHU Montpellier

Montpellier, France

CHRU Nancy

Nancy, France

CHU Rouen

Rouen, France

CHU Saint Etienne

Saint-Etienne, France

CHU Toulouse

Toulouse, France

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NCT06244433


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