Epidural Cortical Stimulation for Depression

Prior treatment

• The EpCS would (in the investigator's judgment) pose an unacceptable surgical or medical risk for the patient (including, but not limited to: history of serious cardiac or pulmonary problems, stroke, significant brain malformation, progressive neurological disease, central nervous system disease or injury, history of seizure, previous neurosurgical procedure with suspected brain tissue scarring that would increase the risks for seizure or cervical fracture).
• Subject received general anesthetic within the last 30 days prior to enrollment (not including ECT procedure).
• Subject currently has another investigational device or cardiac pacemaker, implantable defibrillator, or other implantable stimulator
• Subject is judged by the investigator to be acutely suicidal (e.g. within the 30 days prior to the EpCS implant, the subject has made a suicide attempt or gesture or has made specific plans or preparation to commit suicide).
• Subject with a positive urine drug screen or current alcohol or substance abuse other than nicotine and caffeine.

Other illness

• Subject has a history of schizophrenia, schizoaffective disorder, or other psychotic disorder, active substance abuse or dependence (with the exception to caffeine and nicotine abuse) or a current major depressive episode that includes psychotic features (commonly referred to as psychotic depression) according to the DSM IV criteria.
• Subject with a diagnosis of dementia with a Mini-Mental State Exam (MMSE) ≤23.

Lab values

• Subject on anticoagulant drugs, with low platelets counts or have PT or PTT abnormalities or other risk factors for intra-operative or post-operative bleeding

Other

• The presence of any of the following will exclude a subject from the study:
• Subject is expected to require full body magnetic resonance imaging (MRI) during the clinical study.
• Female subjects with a positive urine pregnancy test.

• To be eligible for this study, a subject must meet all the following inclusion and exclusion criteria:
• Subject has a diagnosis of chronic (≥ two years) or recurrent (multiple prior episodes) depression and is currently experiencing a major depressive episode without psychotic features as defined by DSM IV criteria.
• Subjects may have a diagnosis or unipolar or bipolar depressive episode.
• Subject has not had an adequate response to 4 or more adequate antidepressant treatments in the current depressive episode according to the Antidepressant Treatment History Form (ATHF) (Sackeim et al 1997).
• Subject must be between the ages of 21 and 80.
• Baseline HDRS 24-item ≥ 20 (both visits 1 week apart)
• Subject must be able to complete the evaluations needed for this study including the functional imaging scans.
• Subject must have had a history of one successful course of ECT in the past.
• Subject must provide written informed consent.
• Subject is stable on all antidepressant medication for at least 4 weeks before the baseline visit or not be taking antidepressant medication prior to entering the study.
• Subject must be able to remain on current medication schedule for the first 19 weeks of the study.
• Subject is not on a medication known to increase the risk of cortical stimulation-induced seizures. These include theophylline, stimulant medications, bupropion, or supraphysiological doses of thyroid supplements.