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Recruiting NCT06211348

NCT06211348 Genomic Sequencing in Anatomically Normal Fetuses

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Clinical Trial Summary
NCT ID NCT06211348
Status Recruiting
Phase
Sponsor University of California, San Francisco
Condition Pregnant Individuals Requesting Standard Microarray
Study Type INTERVENTIONAL
Enrollment 1,000 participants
Start Date 2024-01-01
Primary Completion 2029-01

Trial Parameters

Condition Pregnant Individuals Requesting Standard Microarray
Sponsor University of California, San Francisco
Study Type INTERVENTIONAL
Phase N/A
Enrollment 1,000
Sex ALL
Min Age 18 Years
Max Age 64 Years
Start Date 2024-01-01
Completion 2029-01
Interventions
Genomic Sequencing

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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.

Eligibility Criteria

Inclusion Criteria: Pregnant patients who are: * Pregnant with a structurally normal fetus (singleton or multiple gestation) * Planning to undergo prenatal diagnosis by either chorionic villus sampling or amniocentesis with chromosome microarray analysis for routine indications * Planning, or have already completed expanded carrier screening Exclusion Criteria: Pregnant patients who: * Decline prenatal diagnostic testing * Are pregnant and their fetus has a known anomaly * Declined chromosomal microarray analysis of expanded carrier screening

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