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NCT06744543 · ClinicalTrials.gov registry record · NA

Clinical Decision Support to Identify Pediatric Patients With Undiagnosed Genetic Disease

A NA study of Genetic Disease and Pediatrics, sponsored by Vanderbilt University Medical Center.

Active
Registry status
NA
Development phase
1,000
Enrollment target
1
Study location

NCT06744543: Active NA study of Genetic Disease and Pediatrics, sponsored by Vanderbilt University Medical Center.

NCT06744543 is a NA study of Genetic Disease and Pediatrics that is active but no longer recruiting, run by Vanderbilt University Medical Center. 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

NCT06744543, a NA study of Genetic Disease and Pediatrics, is active but no longer recruiting, sponsored by Vanderbilt University Medical Center.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
1,000 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate the effectiveness of SIGHT as a clinical support system to prompt provider/patient discussion and shared decision making regarding the need for genetic testing in the form of a chromosomal microarray. Identifying patients at high predicted probability of needing a test in clinical settings will be examined to determine if it decreases the duration of time to testing and increases diagnostic yield. SIGHT requires only data already collected in routine clinical encounters and is calculated prior to a clinical visit at VUMC.

Primary Outcome

Number of patients diagnosed via a Chromosomal Microarray.

Interventions

  • DEVICE SIGHT Prompted Provider Message

Study Locations (1)

Tennessee

  • Vanderbilt University Medical - Nashville

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2025-03-12
Est. Completion 2027-02-01
Phase NA

What the registry record for NCT06744543 still lists

NCT06744543 is an interventional study that assigns participants to a tested 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 4 conditions, with Genetic Disease appearing as the primary indexed condition, and to 1 intervention - of which SIGHT Prompted Provider Message is the first listed.

NCT06744543 reports a single indexed study location in Tennessee.

Frequently Asked Questions

What is clinical trial NCT06744543 about?

NCT06744543 is a clinical study titled "Clinical Decision Support to Identify Pediatric Patients With Undiagnosed Genetic Disease". This study will evaluate the effectiveness of SIGHT as a clinical support system to prompt provider/patient discussion and shared decision making regarding the need for genetic testing in the form of a chromosomal microarray. Identifying patients at high predicted probability of needing a test in cl...

What is the current status of trial NCT06744543?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 1,000 participants. The study started on 2025-03-12. Estimated completion is 2027-02-01.

What conditions does trial NCT06744543 study?

This clinical trial studies the following conditions: Genetic Disease, Pediatrics, Clinical Decision Support, Predictive Model.

What interventions are being tested in trial NCT06744543?

The interventions under investigation include: SIGHT Prompted Provider Message (DEVICE).

Who is sponsoring clinical trial NCT06744543?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06744543 being conducted?

This trial has 1 study location across Tennessee. 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 NCT06744543'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 NCT06744543, the US trial registry maintained by the National Library of Medicine. NCT06744543 (large enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.