NCT05318222View on ClinicalTrials.gov

Genetic Inclusion by Virtual Evaluation

NARecruitingINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

June 1, 2022

Primary Completion Date

January 31, 2027

Study Completion Date

January 31, 2027

Conditions
Birth DefectsMultiple Congenital AnomalyNeurodevelopmental Disorders
Interventions
DIAGNOSTIC_TEST

Whole genome sequencing (WGS)

WGS will identify copy number variations (CNVs), single nucleotide variants (SNVs), as well as triplet repeat disorders in children with rare diseases

Trial Locations (1)

78539

RECRUITING

University of Texas Rio Grande Valley, Edinburg

All Listed Sponsors
lead

Baylor College of Medicine

OTHER