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Clinical Trial Summary

The investigators aim to determine the feasibility of using the Medtronic LINQ device for epilepsy diagnosis, monitoring and management. The feasibility will be determined by comparing EEG signals from the LINQ system to the gold standard clinical recordings. If seizures can be identified using the LINQ device with the same level of accuracy as adjacent scalp EEG recording electrodes, then the LINQ will be deemed feasible.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03465189
Study type Observational
Source St Vincent's Hospital Melbourne
Contact
Status Completed
Phase
Start date September 10, 2018
Completion date March 19, 2020

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