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NCT03412760 · ClinicalTrials.gov registry record · NA

Hydrops: Diagnosing & Redefining Outcomes With Precision Study

A NA study of Birth Defect and Fetal Anomaly, sponsored by University of California, San Francisco.

Active
Registry status
NA
Development phase
500
Enrollment target
1
Study location

NCT03412760: Active NA study of Birth Defect and Fetal Anomaly, sponsored by University of California, San Francisco.

NCT03412760 is a NA study of Birth Defect and Fetal Anomaly that is active but no longer recruiting, run by University of California, San Francisco. The registered enrollment target is 500 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (64% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03412760, a NA study of Birth Defect and Fetal Anomaly, is active but no longer recruiting, sponsored by University of California, San Francisco.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
500 participants
Enrollment target
1
Study location

Study Summary

This is a national, prospective study designed to investigate the genetic etiologies of non-immune hydrops fetalis (NIHF) and other birth defects. At least half of prenatally diagnosed NIHF cases remain of unknown etiology after standard work up, and a substantial proportion of other birth defects remain of unknown etiology as well. The investigators are performing exome sequencing (ES) for the affected fetus or neonate in unexplained cases, as well as enrolling cases with a genetic explanation to represent the full spectrum of diseases underlying NIHF and other birth defects.

Primary Outcome

Both NIHF and birth defects can be caused by a variety of genetic variants that researchers are continuing to learn more about. Exome sequencing will yield information about the specific genetic variants present in cases of NIHF and other birth defects, and about the specific diseases implicated by these variants. Investigators will determine the proportion of cases seen in the setting of particular genetic variants, and will correlate phenotypic outcomes with specific genotypes.

Interventions

  • DIAGNOSTIC_TEST Exome sequencing

Study Locations (1)

California

  • University of California, San Francisco - San Francisco

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2018-10-11
Est. Completion 2027-02
Phase NA

What the registry record for NCT03412760 still lists

NCT03412760 is an interventional study that assigns participants to a tested intervention. The registered 500 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 (64% lower).

The record links to 3 conditions, with Birth Defect appearing as the primary indexed condition, and to 1 intervention - of which Exome sequencing is the first listed.

NCT03412760 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT03412760 about?

NCT03412760 is a clinical study titled "Hydrops: Diagnosing & Redefining Outcomes With Precision Study". This is a national, prospective study designed to investigate the genetic etiologies of non-immune hydrops fetalis (NIHF) and other birth defects. At least half of prenatally diagnosed NIHF cases remain of unknown etiology after standard work up, and a substantial proportion of other birth defects r...

What is the current status of trial NCT03412760?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 500 participants. The study started on 2018-10-11. Estimated completion is 2027-02.

What conditions does trial NCT03412760 study?

This clinical trial studies the following conditions: Birth Defect, Fetal Anomaly, Hydrops Fetalis.

What interventions are being tested in trial NCT03412760?

The interventions under investigation include: Exome sequencing (DIAGNOSTIC_TEST).

Who is sponsoring clinical trial NCT03412760?

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

Where is trial NCT03412760 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Birth Defect

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03412760's enrollment target sits among peer trials

500 193rd of 2000 higher than 1,788 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 NCT03412760, the US trial registry maintained by the National Library of Medicine. NCT03412760 (mid enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.