NCT06917339招募中不适用
Retrospective Analyses Evaluating the Real-World Effectiveness of NeuroStar® TMS and the Factors Associated With Clinical Outcomes
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- Neuronetics
- 入组人数
- 156,000
- 试验地点
- 1
- 主要终点
- Change in clinical assessment score from baseline to post-treatment
研究概览
简要总结
In this study, real-world data will be used to better understand the effects patient characteristics, symptoms and TMS protocol parameters have on clinical outcomes with NeuroStar TMS.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 5 Years 至 120 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female reported in database and not an invalid entry
- •Age reported and not an invalid entry
- •Treatment date of November 01, 2008 or later.
排除标准
- •Incomplete information on treatment parameters
研究组 & 干预措施
Patients treated with NeuroStar TMS
干预措施: NeuroStar Advanced TMS Therapy System (Device)
结局指标
主要结局
Change in clinical assessment score from baseline to post-treatment
时间窗: 8 weeks
real-world efficacy of NeuroStar TMS in reducing patients' symptoms, reduction in clinical assessment score like PHQ-9
次要结局
- Age at baseline and its correlation to change in score post treatment(8 weeks)
研究者
研究点 (1)
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