NCT00515658Unknown2 期
Antidepressant Effect of Theta-Burst rTMS
适应症
试验速览
- 阶段
- 2 期
- 试验地点
- 2
研究概览
简要总结
The aim of this study is to evaluate the safety and efficacy of theta-burst rTMS in patients with major depression. Patients will be randomized to receive ether left-sided intermittent theta-burst rTMS or rigt-sided continuous theta-burst rTMS or sham theta-burst rTMS over two weeks period with an option for an additional two weeks period, depending on treatment response. Clinical assessments will be performed weekly by the Hamilton depression rating scale. In addition, standard neurophysiological assessment of cortical excitability will be done.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Major depressive episode (DSM IV criteria).
- •Informed consent.
- •Age: 18-70.
排除标准
- •Suicidality
- •Psychosis
- •Pacemaker
- •Cardiac arrythmia
- •seizure disorder
- •implantable metal devices
- •PNS and CNS disorders
- •any other contraindications as specified in safety guidelines for rTMS (Wassermenn, 1998).
研究者
研究点 (2)
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