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Genomic Sequencing in Anatomically Normal Fetuses
Sponsor: University of California, San Francisco
Summary
This cohort study will examine the clinical utility of genomic sequencing (GS) in patients undergoing prenatal diagnostic procedures (chorionic villus sampling or amniocentesis) for routine indications other than a structural fetal anomaly.
Key Details
Gender
All
Age Range
18 Years - 64 Years
Study Type
INTERVENTIONAL
Enrollment
1000
Start Date
2024-01-01
Completion Date
2030-01
Last Updated
2026-04-08
Healthy Volunteers
Yes
Interventions
Genomic Sequencing
Individuals who request prenatal diagnostic testing with standard chromosomal microarray will be offered genomic sequencing (GS) as an option to assess for additional disease risk.
Locations (1)
University of California, San Francisco
San Francisco, California, United States