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NCT03458962 · ClinicalTrials.gov registry record

Diagnostic Odyssey: Whole Genome Sequencing (WGS)

A clinical trial of Genetic Disease and Genetic Syndrome, sponsored by Nicklaus Children's Hospital f/k/a Miami Children's Hospital.

Recruiting
Registry status
1,000
Enrollment target
1
Study location

NCT03458962: Recruiting study of Genetic Disease and Genetic Syndrome, sponsored by Nicklaus Children's Hospital f/k/a Miami Children's Hospital.

NCT03458962 is a study of Genetic Disease and Genetic Syndrome that is actively recruiting participants, run by Nicklaus Children's Hospital f/k/a Miami Children's Hospital. The registered enrollment target is 1,000 participants, below the 2,528-participant average among 30 other Genetic Disease trials with a reported enrollment target (60% 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

NCT03458962, a study of Genetic Disease and Genetic Syndrome, is actively recruiting participants, sponsored by Nicklaus Children's Hospital f/k/a Miami Children's Hospital.

RECRUITING
Registry status
1,000 participants
Enrollment target
1
Study location

Study Summary

The goal of this collaborative research is to study human genomes in children with suspected congenital disease, multiple-congenital anomalies and/or multi-organ disease of unknown etiology by understanding the potential value of Whole Genome Sequencing (WGS) in establishing genetic diagnosis. The study will examine diagnosis rates, changes in clinical care as a result of a genetic diagnosis, health economics including potential cost-effectiveness of WGS and patient and provider experience with genomic medicine.

Primary Outcome

Total number of enrolled patients who will undergo WGS testing

Interventions

  • GENETIC Genetic Enrollees

Study Locations (1)

Florida

  • Nickalus Children's Hospital f/k/a Miami Children's Hospital - Miami

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2018-02-20
Est. Completion 2070-03

What NCT03458962 shows while recruiting

NCT03458962 is an observational study that tracks outcomes without assigning an intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus, below the 2,528-participant average among 30 other Genetic Disease trials with a reported enrollment target (60% lower).

The record links to 2 conditions, with Genetic Disease appearing as the primary indexed condition, and to 1 intervention - of which Genetic Enrollees is the first listed.

NCT03458962 reports a single indexed study location in Florida.

Frequently Asked Questions

What is clinical trial NCT03458962 about?

NCT03458962 is a clinical study titled "Diagnostic Odyssey: Whole Genome Sequencing (WGS)". The goal of this collaborative research is to study human genomes in children with suspected congenital disease, multiple-congenital anomalies and/or multi-organ disease of unknown etiology by understanding the potential value of Whole Genome Sequencing (WGS) in establishing genetic diagnosis. The s...

What is the current status of trial NCT03458962?

This trial is currently recruiting. The enrollment target is 1,000 participants. The study started on 2018-02-20. Estimated completion is 2070-03.

What conditions does trial NCT03458962 study?

This clinical trial studies the following conditions: Genetic Disease, Genetic Syndrome.

What interventions are being tested in trial NCT03458962?

The interventions under investigation include: Genetic Enrollees (GENETIC).

Who is sponsoring clinical trial NCT03458962?

This trial is sponsored by Nicklaus Children's Hospital f/k/a Miami Children's Hospital, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03458962 being conducted?

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

Similar trials for Genetic Disease

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 NCT03458962's enrollment target sits among peer trials

1,000 6th of 30 higher than 24 of 30 other Genetic Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Genetic Disease 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 NCT03458962, the US trial registry maintained by the National Library of Medicine. NCT03458962 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.