Accelerometer Device
DeviceA sensor platform that enables physiological monitoring in routine, home or office environments.
NCT Number: NCT01612689
This is a prospective, unblinded sub-study to the E-30 to gather physiological data.
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Notify Me6 year and older
All sexes
Interventional
Not applicable
Gainesville, Florida, United States
This sub-study to the E-30 is designed to collect vital signs, accelerometer and ECG data on subjects, and will consist of two phases. Phase 1 is designed to collect data in an Epilepsy Monitoring Unit (EMU) and Phase 2 is designed to collect data in an everyday (ambulatory) setting.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(Phase 1)
(Phase 1&2)
(Sleep State: Optional)
Exclusion criteria
(Phase 1&2)
(Sleep State: Optional)
A sensor platform that enables physiological monitoring in routine, home or office environments.
Time frame: Up to 2 weeks
The purpose of this sub-study is to gather physiological data in consenting subjects who were previously enrolled in the "parent" E-30 study (NCT01202669).
Cyberonics, Inc.
Industry
3-Dimensional Accelerometer Sub-Study for Patients Participating in the E-30 Study: Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission
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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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