Genetic Inclusion by Virtual Evaluation
Recruiting now · Not applicable
Conditions studied: Birth Defects, Multiple Congenital Anomaly, Neurodevelopmental Disorders
In brief
This study aims to transform the current clinical practice paradigm by leveraging an internally designed web-based model of delivery of care called Consultagene to provide remote evaluation and genomic sequencing for improving genetic health of less resourced children with rare disorders living along the Texas-Mexico border.
Key facts
- Study ID
- NCT05318222
- Run by
- Baylor College of Medicine
- People needed
- 200
- Starts
- 2022-06-01
- Expected to finish
- 2027-01-31
- Last updated by the study team
- 2025-01-30
Who can join
Age: 0 and older, up to 18. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Pediatric patients with undiagnosed rare genetic diseases residing in the Rio Grande Valley and El Paso in Texas
You may not qualify if…
- Children with known genetic diseases
Where it is running
- University of Texas Rio Grande Valley — Edinburg, Texas, United States (enrolling)
Full record on ClinicalTrials.gov
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