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Sponsored by: |
Mayo Clinic |
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Information provided by: | Mayo Clinic |
ClinicalTrials.gov Identifier: | NCT00587951 |
The aim of this study is to determine the role of SISCOM (see below) in aiding clinicians to manage epilepsy surgery candidates. SISCOM is already a routine component of pre-surgical epilepsy evaluation at Mayo Clinic. In particular, we are interested in assessing whether use of SISCOM can minimize the need for prolonged (>24 hours) invasive monitoring with electrodes placed on the surface of the brain prior to surgical resection.
Note: this study has recruited the required number of patients and is closed to further enrolment.
Condition |
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Epilepsy |
Study Type: | Observational |
Study Design: | Case-Only, Prospective |
Official Title: | The Influence of SISCOM on Intracranial Electrode Implantation in Epilepsy Surgical Candidates |
Enrollment: | 50 |
Study Start Date: | December 2005 |
Study Completion Date: | February 2007 |
Primary Completion Date: | February 2007 (Final data collection date for primary outcome measure) |
Groups/Cohorts |
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A
Candidates for epilepsy surgery, undergoing pre-surgical evaluation at Mayo Clinic, and in whom SISCOM was ordered by the treating physician as part of that evaluation
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Successful epilepsy surgery depends on accurate identification of the area of brain from which seizures originate (the epileptogenic zone). There are many non-invasive tests (including EEG and MRI) to indicate this area. Some patients require implantation of intracranial electrodes in order to determine the epileptogenic zone. A test known as SISCOM (subtraction ictal-interictal SPECT co-registered with MRI) has been validated as a non-invasive means of indicating the epileptogenic zone. However, this test is not widely available in the US, and it is not known how often the additional information provided by SISCOM makes a difference to clinical decision-making.
In order to determine the contribution of SISCOM towards clinical decision-making in epilepsy surgery candidates, we will ask epileptologists at Mayo Clinic to consider case presentations given all clinical information except for SISCOM results, and then to reconsider those same cases in conjunction with SISCOM data. This will indicate the degree to which SISCOM influences decision making.
50 patients at Mayo Clinic (38 adults, 12 children) will be enrolled.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Patients evaluated at Mayo Clinic and being considered for epilepsy surgery.
Inclusion Criteria:
Responsible Party: | Mayo Foundation ( Dr. K. Meng Tan ) |
Study ID Numbers: | 2170-05 |
Study First Received: | December 22, 2007 |
Last Updated: | January 7, 2008 |
ClinicalTrials.gov Identifier: | NCT00587951 |
Health Authority: | United States: Institutional Review Board |
Clinical decision-making Ictal SPECT Epilepsy surgery |
Epilepsy Central Nervous System Diseases Brain Diseases |
Nervous System Diseases |