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Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

Recruitingn/aAges any - anyAllNantes University Hospital
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In plain words

What the trial is, and whether it could suit you

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

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Child Inclusion Criteria * 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 * Children who also meet the inclusion criteria for the BIOMINRISK-NEUROBIO (axis 2) and BIOMINRISK-RADIO-ANAT (axis 3) studies in the overall BIOMINRISK project. Parents Inclusion Criteria * 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 Child Exclusion Criteria: * 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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What it tests

  • whole genome sequencing
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Where

18 sites
Nantes University Hospital
Nantes, France
CHU Amiens
Amiens, France
CHU Angers
Angers, France
CHU Besançon
Besançon, France
APHP - Hôpital Jean Verdier
Bondy, France
CHU Brest
Brest, France
CHU de Caen-Normandie
Caen, France
APHP - Hôpital Antoine Béclère
Clamart, France

…and 10 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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