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OpenTrials
Completed

NCT Number: NCT01202669

Heart Rate Changes in Subjects With Epilepsy

The purpose of this study is to collect continuous observational data during a clinical Epilepsy Monitoring Unit evaluation.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Florida, Gainesville, Florida, United States

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About this study

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.

Who can participate

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:

  • Patient has a clinical diagnosis of epilepsy requiring evaluation in an epilepsy monitoring unit (EMU).
  • Patient likely requires an EMU evaluation for a period of at least 24 hours.
  • Patient is currently taking at least one antiepileptic medication.
  • Patient must be in good general health and fully ambulatory.
  • Patient or guardian must be willing and able to complete informed consent/assent and HIPAA authorization.

Exclusion criteria

Patients who meet any of the following criteria are not eligible to be enrolled in the study:

  • Patients with severe psychiatric disease that in the investigator's judgment would prevent the patient's successful completion of the study.
  • Patients with a history of status epilepticus.
  • Patients prescribed drugs specifically for a cardiac or autonomic disorder that in the investigator's opinion would affect heart rate response. Drugs with secondary cardiac or autonomic actions are allowed.
  • Patients with cardiovascular arrhythmias or cardiac disease that would preclude the ability to detect intrinsic changes in heart rate due to exercise, stress, or seizure. This would include but not be limited to chronic atrial fibrillation, chronotropic incompetence, and permanent cardiac pacemaker implantation.
  • Patients with a history of dependence on alcohol or narcotic drugs within the past 2 years as defined by DSM IV-R.

Treatment and study plan

No intervention planned, observational study only.

Other

No intervention planned, observational study only.

Primary outcomes

  1. Collection of physiologic data during an Epilepsy Monitoring Unit (EMU) stay

    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.

Sponsors and collaborators

Lead sponsor

Cyberonics, Inc.

Industry

Registry information

Official study title

Heart Rate Changes in Subjects With Epilepsy During an Epilepsy Monitoring Unit Admission

Important dates

Study start
2010
Primary completion
2012
Study completion
2014
First posted
Sep 16, 2010
Registry last updated
Aug 7, 2014

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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