Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

Recruiting now

Conditions studied: Sudden Infant Death, Sudden Unexplained Infant Death

In brief

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

Key facts

Study ID

NCT06244433

Run by

Nantes University Hospital

People needed

650

Starts

2024-08-27

Expected to finish

2027-10-27

Last updated by the study team

2026-06-18

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

• CHU Toulouse — Toulouse, France (enrolling)
• CHU Amiens — Amiens, France (enrolling)
• CHU Angers — Angers, France (enrolling)
• CHU Besançon — Besançon, France (enrolling)
• APHP - Hôpital Jean Verdier — Bondy, France (enrolling)
• CHU Brest — Brest, France (enrolling)
• CHRU Nancy — Nancy, France (enrolling)
• CHU Rouen — Rouen, France (enrolling)
• CHU Saint Etienne — Saint-Etienne, France (enrolling)
• Nantes University Hospital — Nantes, Loire-Atlantique, France (enrolling)
• APHP - Hôpital Antoine Béclère — Clamart, France (enrolling)
• CHU Grenoble — Grenoble, France (enrolling)
• HCL — Lyon, France (enrolling)
• CHU Montpellier — Montpellier, France (enrolling)
• CHU de Caen-Normandie — Caen, France
• CHU de Poitiers — Poitiers, France
• Centre Hospitalier Sud Francilien — Corbeil-Essonnes, France
• AP-HM — Marseille, France

Full record on ClinicalTrials.gov

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