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Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome
Sponsor: Nantes University Hospital
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
Official title: Risk Stratification of Sudden Unexpected Death in Infant Based on Biomarkers - Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
650
Start Date
2024-08-27
Completion Date
2027-10
Last Updated
2025-01-31
Healthy Volunteers
No
Interventions
whole 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