Mayo Clinic Institutional Review Board, Phoenix VA Health Care System Institutional Review Board, and U.S. Department of Defense Human Research Protection Office approvals were obtained prior to initiation of study procedures.
EEG signals provide important information about epileptogenic networks that must be analyzed and understood before the initiation of therapeutic procedures.
Reasons why patients were not contacted through the Outreach Program include insufficient or inaccurate locator information or the patient returned to clinic prior to the initiation of outreach procedures.
All patients provided written informed consent before initiation of study procedures.
Written informed consent was obtained from each subject before initiation of study procedures.
All patients and healthy controls signed a consent form prior to initiation of study procedures.
Informed parental permission and subject assent were obtained prior to initiation of study procedures.
Patient consent must be obtained prior to the registration or initiation of trial procedures.
Informed consent was obtained from all participants prior to the initiation of study procedures.
Oral assent was also obtained from all the participating children prior to the initiation of study procedures.
