New study aims to speed up rare disease diagnosis for newborns in rural texas
NCT ID NCT07102966
First seen Sep 30, 2025 · Last updated Jun 11, 2026 · Updated 39 times
Summary
This study offers rapid whole genome sequencing and virtual genetic consultations to 200 seriously ill newborns in hospitals with fewer resources, especially along the Texas-Mexico border. Researchers want to see if the virtual tool Consultagene helps doctors diagnose rare diseases faster than usual care. The goal is to improve access to advanced testing and gather feedback from healthcare providers.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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Baylor College of Medicine
RECRUITINGHouston, Texas, 77030, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
The condition(s) this trial relates to.
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