Genomic Sequencing in Anatomically Normal Fetuses
University of California, San Francisco · NCT06211348
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–64 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 1000
- US sites recruiting
- 1
- Study start
- January 1, 2024
- Record last updated
- April 8, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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.
Being studied: Genomic Sequencing
Conditions: Pregnant Individuals Requesting Standard Microarray
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full 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
Recruiting US locations
University of California, San Francisco
San Francisco, CA 94143
Site contact: Nuriye Sahin Hodoglugil, DrPH · Nuriye.Sahin-Hodoglugil@ucsf.edu
Study contacts (from the official record)
- Nuriye Sahin Hodoglugil, DrPH · 415-353-3400 · Nuriye.Sahin-Hodoglugil@ucsf.edu
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