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NCT07610590 · ClinicalTrials.gov registry record

guideSEQ: Genomic Understanding, Impact, Decision & Ethics in Prenatal Sequencing

A clinical trial, sponsored by Columbia University.

Recruiting
Registry status
1,042
Enrollment target

NCT07610590: Recruiting study, sponsored by Columbia University.

NCT07610590 is a clinical trial that is actively recruiting participants, run by Columbia University. The registered enrollment target is 1,042 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07610590 is actively recruiting participants, sponsored by Columbia University.

RECRUITING
Registry status
1,042 participants
Enrollment target

Study Summary

This study looks at whether genome sequencing should be used more routinely during pregnancy, even when ultrasounds look normal. Genome sequencing can examine nearly all of a baby's genes and may find genetic conditions that standard tests do not detect. Researchers will compare this test with current prenatal testing to see if it provides helpful information for families and doctors. The study will also explore how parents decide what kinds of genetic information they want to receive and how this information affects their experience during pregnancy. The goal is to understand whether genome sequencing can be used in a way that is helpful, responsible, and supportive for families in the future.

Primary Outcome

The incremental frequency of fetal genetic conditions identified and reported by genomic sequencing (GS) compared to those found by standard-of-care (SOC) testing, including pathogenic, likely pathogenic, or variant of uncertain significance (VUS) variants identified by sequencing and deemed reportable by the Variant Adjudication Committee

Interventions

  • GENETIC Genome Sequencing (GS)

Trial Details

FieldValue
Enrollment Target 1,042 participants
Start Date 2026-04-29
Est. Completion 2029-07-31
Columbia University

958 total trials

What NCT07610590 shows while recruiting

NCT07610590 is an observational study that tracks outcomes without assigning an intervention. Its 1,042 participants enrollment target places it among the larger protocols in the corpus.

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

NCT07610590 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07610590 about?

NCT07610590 is a clinical study titled "guideSEQ: Genomic Understanding, Impact, Decision & Ethics in Prenatal Sequencing". This study looks at whether genome sequencing should be used more routinely during pregnancy, even when ultrasounds look normal. Genome sequencing can examine nearly all of a baby's genes and may find genetic conditions that standard tests do not detect. Researchers will compare this test with curre...

What is the current status of trial NCT07610590?

This trial is currently recruiting. The enrollment target is 1,042 participants. The study started on 2026-04-29. Estimated completion is 2029-07-31.

What interventions are being tested in trial NCT07610590?

The interventions under investigation include: Genome Sequencing (GS) (GENETIC).

Who is sponsoring clinical trial NCT07610590?

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

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Source: ClinicalTrials.gov NCT07610590, the US trial registry maintained by the National Library of Medicine. NCT07610590 (large enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.