NCT06244433View on ClinicalTrials.gov

Identification of Genetic Variants Associated With Unexpected Infant Death Syndrome

RecruitingOBSERVATIONAL
Enrollment

650

Participants

Timeline

Start Date

August 27, 2024

Primary Completion Date

August 31, 2026

Study Completion Date

October 31, 2027

Conditions
Sudden Infant DeathSudden Unexplained Infant Death
Interventions
GENETIC

whole genome sequencing

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

Trial Locations (15)

44093

RECRUITING

Nantes University Hospital, Nantes

Unknown

RECRUITING

CHU Amiens, Amiens

RECRUITING

CHU Angers, Angers

RECRUITING

CHU Besançon, Besançon

RECRUITING

APHP - Hôpital Jean Verdier, Bondy

RECRUITING

CHU Brest, Brest

RECRUITING

APHP - Hôpital Antoine Béclère, Clamart

RECRUITING

CHU Grenoble, Grenoble

RECRUITING

HCL, Lyon

NOT_YET_RECRUITING

AP-HM, Marseille

RECRUITING

CHU Montpellier, Montpellier

RECRUITING

CHRU Nancy, Nancy

RECRUITING

CHU Rouen, Rouen

RECRUITING

CHU Saint Etienne, Saint-Etienne

RECRUITING

CHU Toulouse, Toulouse

All Listed Sponsors
collaborator

AXA Assurances VIE Mutuelle

UNKNOWN

collaborator

Institut du Thorax

UNKNOWN

lead

Nantes University Hospital

OTHER