NCT03831035View on ClinicalTrials.gov

Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit

CompletedOBSERVATIONAL
Enrollment

45

Participants

Timeline

Start Date

April 8, 2019

Primary Completion Date

June 8, 2022

Study Completion Date

June 8, 2022

Conditions
Infant, Newborn, DiseasesCongenital MalformationsIntensive Care UnitNeurologic Symptoms
Interventions
OTHER

Genetic analyse by whole exome sequencing

Exome sequencing requires analytic, bio informatic and interpretation steps.

Trial Locations (1)

34295

Medical genetics Arnaud de Villeneuve, Montpellier

All Listed Sponsors
lead

University Hospital, Montpellier

OTHER

NCT03831035 - Fast Exome for Diagnosis of Congenital Conditions in Infants Under 12 Months of Age Hospitalized in Intensive Care Unit | Biotech Hunter | Biotech Hunter