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Clinical Trial

Genomic Sequencing in Anatomically Normal Fetuses

NCT: NCT06211348 · RECRUITING

NCT IDNCT06211348
StatusRECRUITING
Start Date2024-01-01

Brief 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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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