NCT01343732Unknown不适用
Tolerability, Safety and Efficacy of the HAC-Coil Deep Transcranial Magnetic Stimulation in Medication Resistance Obsessive Compulsive Disorder (OCD) Subjects
适应症
试验速览
- 阶段
- 不适用
- 发起方
- Brainsway
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Y-BOCS Scale (Yale-Brown Obsessive Compulsive Disorder)
研究概览
简要总结
The purpose of this study is to test whether the combination of deep transcranial magnetic stimulation (DTMS) treatment with customary medication for obsessive compulsive disorder (OCD) patients is effective than treatment that include only medication.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Outpatients
- •Men and Women 18-65 years of age.
- •Diagnosed as suffering from OCD according to DSM-IV.
- •Patients having OCD of at least moderate severity (YBOCS score of 20 or above).
- •Patients are maintained on an medication at steady dosages for at least 8 weeks before study entry and for the duration of the trail.
- •Negative answers on safety screening questionnaire for transcranial magnetic stimulation.
- •According to the treating physician the patients is compliant with taking medication.
- •Capable and willing to provide informed consent.
- •Able to adhere to treatment schedule.
- •Patients that participate in behavioral therapy, will be in the maintaining stage and not in the active or intensive stage.
排除标准
- •Any other Axis I diagnosis as the primary diagnosis.
- •History of epilepsy or seizure (EXCEPT those therapeutically induced by ECT) or history of such in first degree relatives).
- •OCD patients that have only symptoms of hoarders)
- •patients with Suicidal tendencies, or the patients is diagnosed as having a Suicidal tendencies by the treating physician.
- •Increased risk of seizure for any reason, including prior diagnosis of increased intracranial pressure, or history of significant head trauma with loss of consciousness for greater than or equal to 5 minutes.
- •History of head injury necessitating cranial surgery or prolonged coma.
- •History of any metal in the head including the eyes and ears (outside the mouth).
- •Known history of any metallic particles in the eye, implanted cardiac pacemaker or any intracardiac lines, implanted neurostimulators, intracranial implant (e.g., aneurysm clips, shunts, stimulators, cochlear implants, or electrodes) or implanted medical pumps.
- •History of frequent or severe headaches.
- •History of migraine.
- •History of significant hearing loss.
- •Individuals with a significant neurological disorder or insult including, but not limited to:
- •Any condition likely to be associated with increased intracranial pressure Space occupying brain lesion History of cerebrovascular accident Transient ischemic attack within two years Cerebral aneurysm Dementia Parkinson's disease Huntington's chorea Multiple sclerosis
- •History of substance abuse including alcoholism within the past 6 months (except nicotine and caffeine).
- •Inadequate communication with the patient.
- •Participation currently in another clinical study or enrolled in another clinical study within 30 days prior to this study.
- •Participants who suffer from an unstable physical, systemic and metabolic disorders such as instabilized blood pressure or acute, unstable cardiac disease.
- •Women who are breast-feeding.
- •Known or suspected pregnancy.
- •Women of childbearing potential and not using a medically accepted form of contraception when engaging in sexual intercourse.
结局指标
主要结局
Y-BOCS Scale (Yale-Brown Obsessive Compulsive Disorder)
时间窗: the primary outcome will be measure at day, 8, 22, 31, and 33
次要结局
未报告次要终点
研究者
研究点 (1)
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