Refining Information Technology Support for Genetics in Medicine

Status unconfirmed

Conditions studied: Hypertrophic Cardiomyopathy, Hearing Loss, Cancer

In brief

The clinical use of genetic testing is expanding and, as a result, the number of variants identified in patients is growing. Knowledge of the clinical impact of these variants improves over time. However, the combination of more testing and the rapid evolution of genetic knowledge make it impossible for clinicians to fully account for the latest implications of their patients' genetic profiles as patient care decisions are made. This proposed study plans to enhance and evaluate IT infrastructure developed to provide timely genetic variant updates and patient search functionality to clinicians to assist in optimizing patient care.

Key facts

Study ID
NCT01225978
Run by
Brigham and Women's Hospital
People needed
40
Starts
2009-09-01
Expected to finish
2014-12-01
Last updated by the study team
2014-01-24

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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