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RECRUITING
NCT06244433

Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

Sponsor: Nantes University Hospital

View on ClinicalTrials.gov

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

GENETIC

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