Condition: Genetic Disease · Genetic Syndrome · Sponsor: Nicklaus Children's Hospital f/k/a Miami Children's Hospital
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.
This description comes directly from the study's public registry record.
Diana Soler, CRC · 786-624-2548 · diana.soler@nicklaushealth.org
Jenny Esteves, MBA/MHSA · 786-624-2854 · jenny.esteves@nicklaushealth.org
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| Nickalus Children's Hospital f/k/a Miami Children's Hospital | Miami, Florida, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT03458962