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NCT03936101 · ClinicalTrials.gov registry record

Prenatal Genetic Diagnosis by Genomic Sequencing

A clinical trial, sponsored by Columbia University.

Completed
Registry status
1,097
Enrollment target

NCT03936101 is a clinical trial that has completed, run by Columbia University. The registered enrollment target is 1,097 participants.

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The verdict

NCT03936101 has completed, sponsored by Columbia University.

COMPLETED
Registry status
1,097 participants
Enrollment target

Study Summary

This study is evaluating the impact of prenatal sequencing on the management of fetuses with ultrasound abnormalities. The hypothesis is that a significant subset of fetal abnormalities have a genetic cause that can be identified by sequencing and that prenatal knowledge of this information will improve prenatal care, reduce unnecessary diagnostic testing, reduce the cost of care, and improve the quality of life for both the child and the family.

Interventions

  • DIAGNOSTIC_TEST Prenatal Genomic Sequencing

Trial Details

FieldValue
Enrollment Target 1,097 participants
Start Date 2019-06-28
Est. Completion 2024-03-25

Sponsor

Columbia University

958 total trials

What the Registry Record Tells You About NCT03936101

The ClinicalTrials.gov registry entry for NCT03936101 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 1,097 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Prenatal Genomic Sequencing is the first listed.

NCT03936101 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03936101 about?

NCT03936101 is a clinical study titled "Prenatal Genetic Diagnosis by Genomic Sequencing". This study is evaluating the impact of prenatal sequencing on the management of fetuses with ultrasound abnormalities. The hypothesis is that a significant subset of fetal abnormalities have a genetic cause that can be identified by sequencing and that prenatal knowledge of this information will imp...

What is the current status of trial NCT03936101?

This trial is currently completed. The enrollment target is 1,097 participants. The study started on 2019-06-28. Estimated completion is 2024-03-25.

What interventions are being tested in trial NCT03936101?

The interventions under investigation include: Prenatal Genomic Sequencing (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT03936101?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.