No intervention planned, observational study only.
OtherNo intervention planned, observational study only.
NCT Number: NCT01202669
The purpose of this study is to collect continuous observational data during a clinical Epilepsy Monitoring Unit evaluation.
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Observational
University of Florida, Gainesville, Florida, United States
Observational, unblinded, non-randomized, multisite study designed to collect data on up to 500 subjects undergoing evaluation for epilepsy in EMUs. Subjects currently enrolled or that previously participated in this study may be eligible for the E-30-S sub-study.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Patients enrolled in the study must meet all of the following criteria:
Exclusion criteria
Patients who meet any of the following criteria are not eligible to be enrolled in the study:
No intervention planned, observational study only.
Time frame: up to 7 days
To collect continuous observational video, electroencephalogram (EEG), electrooculogram (EOG), and electrocardiogram (ECG) data during ictal and non-ictal events occurring over a clinical EMU evaluation.
Cyberonics, Inc.
Industry
Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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