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NCT03482141 · ClinicalTrials.gov registry record · NA

Clinical Utility of Prenatal Whole Exome Sequencing

A NA study, sponsored by University of California, San Francisco.

Completed
Registry status
NA
Development phase
316
Enrollment target

NCT03482141: Completed NA study, sponsored by University of California, San Francisco.

NCT03482141 is a NA study that has completed, run by University of California, San Francisco. The registered enrollment target is 316 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03482141, a NA study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
NA
Development phase
316 participants
Enrollment target

Study Summary

The investigator aims to examine the clinical utility of WES, including assessment of a variety of health-related and reproductive outcomes in undiagnosed prenatal cases.

Primary Outcome

Number of prenatal patients (pregnancies with a structural anomaly) who got a positive exome result among those who had the exome test. Positive exome result is defined as identification of definitive or probable positive variants which explain prenatal phenotype.

Interventions

  • DEVICE Whole Exome Sequencing (WES)

Trial Details

FieldValue
Enrollment Target 316 participants
Start Date 2017-08-01
Est. Completion 2022-05-13
Phase NA

What the finished NCT03482141 record still lists

NCT03482141 is an interventional study that assigns participants to a tested intervention. The registered 316 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which Whole Exome Sequencing (WES) is the first listed.

NCT03482141 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03482141 about?

NCT03482141 is a clinical study titled "Clinical Utility of Prenatal Whole Exome Sequencing". The investigator aims to examine the clinical utility of WES, including assessment of a variety of health-related and reproductive outcomes in undiagnosed prenatal cases.

What is the current status of trial NCT03482141?

This trial is currently completed. It is a NA study. The enrollment target is 316 participants. The study started on 2017-08-01. Estimated completion is 2022-05-13.

What interventions are being tested in trial NCT03482141?

The interventions under investigation include: Whole Exome Sequencing (WES) (DEVICE).

Who is sponsoring clinical trial NCT03482141?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03482141's enrollment target sits among peer trials

316 321st of 2000 higher than 1,678 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03482141, the US trial registry maintained by the National Library of Medicine. NCT03482141 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.