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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Identification of Genetic Variants Associated With Unexpected Infant Death SyndromeDeath, Death, Sudden, Infant Death, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Sudden Infant DeathRecruitingNot stated2026-06-18NCT06244433

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Research sitesCityCountryLinked trials
AP-HMMarseilleFrance13
APHP - Hôpital Antoine BéclèreClamartFrance1
APHP - Hôpital Jean VerdierBondyFrance1
Centre Hospitalier Sud FrancilienCorbeil-EssonnesFrance13
CHRU NancyNancyFrance31
CHU AmiensAmiensFrance49
CHU AngersAngersFrance87
CHU BesançonBesançonFrance32
CHU BrestBrestFrance37
CHU de Caen-NormandieCaenFrance1
CHU de PoitiersPoitiersFrance40
CHU GrenobleGrenobleFrance48
CHU MontpellierMontpellierFrance56
CHU RouenRouenFrance49
CHU Saint EtienneSaint-EtienneFrance22
CHU ToulouseToulouseFrance76
HCLLyonFrance13
Nantes University HospitalNantesFrance17