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| Sponsor: | Infinite Biomedical Technologies |
|---|---|
| Collaborators: |
National Heart, Lung, and Blood Institute (NHLBI) Johns Hopkins Bloomberg School of Public Health Johns Hopkins University Medical College of Wisconsin Virginia Commonwealth University |
| Information provided by: | Infinite Biomedical Technologies |
| ClinicalTrials.gov Identifier: | NCT00483873 |
Purpose
The purpose of the study is to collect EEG's as close to the cardiac arrest as possible using a standard hospital EEG machine and an investigational EEG device to help determine the neurological status of the cardiac arrest patient and to help decide on possible treatment and chance of recovery. The investigational EEG machine will be simple to operate as well as easy to interpret for the clinician and the nurses. It is not to replace the electrophysiologist interpretation but to determine ealy on if further evaluation and treatment can help the patient.
| Condition |
|---|
|
Cardiac Arrest Arrhythmia |
| Study Type: | Observational |
| Study Design: | Observational Model: Case Control Time Perspective: Prospective |
| Official Title: | Phase IIB Study of Novel Quantitative Neurodiagnostic Technology in the Early Period After Cardiac Arrest |
| Estimated Enrollment: | 100 |
| Study Start Date: | August 2007 |
| Estimated Study Completion Date: | December 2009 |
Cardiac arrest claims over 450,000 lives per year in the United States alone. There is a high incidence of neurological complications amongst survivors, and these represent the leading cause of morbidity.
Over the past several years, the care of these patients has been improved via the introduction of new systemic as well as neurospecific therapies. Speed of institution of therapy appears to be an important factor affecting efficacy. Yet, in the crucial initial hours to days post-arrest, assessment of neurological status in these patients is essentially non-existent.
Thus, there is a need for an objective validated tool to assess prognosis and to track neurological status in the early recovery period. In response to this need, we have developed an EEG based Cortical Health Index (CHI). This EEG-based index incorporates multiple weighted parameters derived from 2 channels (4 scalp electrodes + 1 ground electrode) which are related to neurologic functional recovery. The strength and uniqueness of this approach results from consideration of both the temporal as well as the spectral domains of EEG. Our Phase II results demonstrate that CHI measured within the first 6-hours post-arrest resuscitation is strongly correlated with clinical outcome at hospital discharge in a 30-patient cardiac arrest study. Together with our industry collaborator, we now propose to pursue regulatory approval of the CHI Monitor. Our plan involves a prospective clinical trial involving 4 centers and 100 patients (64 Cardiac Arrest Patients and 36 patients undergoing ICD placement as controls). We will test the ability of CHI to: 1) provide early prediction of subsequent neurological functional outcome of cardiac arrest patients, and 2) provide real-time tracking of brain injury and response to therapy. Successful completion of this project is defined by FDA clearance of the CHI Monitor.
It is our goal that the CHI Monitor will identify patients who could benefit from aggressive intervention, and then track the response to the therapy. Providing this information to the treating physician in the immediate post-resuscitation period represents a major change in care delivery for the cardiac arrest survivor.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Patients admitted to the hospital after out-of-hospital Cardiac arrest or for an ICD placement
Inclusion Criteria:
Cardiac Arrest:
Patients 18 years and older:
ICD patients:
Patients 18 years and older:
Exclusion Criteria:
Cardiac Arrest:
ICD patients:
Contacts and Locations| Contact: Romergryko Geocadin, MD | 410-614-6145 | rgeocadi@jhmi.edu |
| United States, Maryland | |
| Johns Hopkins Hospital | Recruiting |
| Baltimore, Maryland, United States, 21187 | |
| Contact: Daniel F Hanley, MD 410-614-6996 dhanley@jhmi.edu | |
| Principal Investigator: Romergryko Geocadin, MD | |
| Johns Hopkins Bayview Medical Center | Recruiting |
| Baltimore, Maryland, United States, 21224 | |
| Principal Investigator: Romergryko Geocadin, MD | |
| United States, Virginia | |
| Virginia Commonwealth University | Not yet recruiting |
| Richmond, Virginia, United States, 23298 | |
| Contact: Mary Ann Peberdy, MD 804-828-4571 mpeberdy@aol.com | |
| Principal Investigator: Mary Ann Peberdy, MD | |
| United States, Wisconsin | |
| Medical College of Wisconsin at Froedtert Memorial Luthern Hospital Clinics - Neurology | Recruiting |
| Milwaukee, Wisconsin, United States, 53226 | |
| Contact: Michel Torbey, MD,MPH 414-805-5343 mtorbey@mcw.edu | |
| Principal Investigator: Michel Torbey, MD, MPH | |
| Principal Investigator: | Neil S Rothman, PhD | Infinite Biomedical Technologies - Study Sponsor |
| Principal Investigator: | Romergryko Geocadin, MD | Johns Hopkins Medical Institutions |
| Principal Investigator: | Michel Torbey, MD, MPH | Medical College of Wisconsin |
| Principal Investigator: | Mary Ann Peberdy, MD | Virginia Commonwealth University |
More Information
| Responsible Party: | Dr. Neil Rothman, Vice-President of Research and Development, IInfinite Biomedical Technologies, llc |
| ClinicalTrials.gov Identifier: | NCT00483873 History of Changes |
| Other Study ID Numbers: | R44HL070129, R44HL070129 |
| Study First Received: | June 6, 2007 |
| Last Updated: | January 28, 2009 |
| Health Authority: | United States: Institutional Review Board |
|
Cardiac Arrest, Neurological Recovery, EEG, Quantitative EEG |
|
Arrhythmias, Cardiac Heart Arrest Heart Diseases Cardiovascular Diseases Pathologic Processes |