跳至主要内容
临床试验/jRCTs042180154
jRCTs042180154招募中不适用

Study of efficasy and effect prediction of Repetitive Transcranial Magnetic Stimulation in psychiatric disorder. (rTMS)

未提供0 个研究点目标入组 50 人开始时间: 2015年9月7日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
50
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Single Arm Study
干预模型
Single Assignment
主要目的
Prevention Purpose
盲法
Open(masking Not Used)

入排标准

年龄范围
20age old over 至 80age old under(—)
性别
All

入选标准

  • Patients who has diagnosis of depressed disorder group, bipolar disorder and related disorder group, schizophrenia spectrum disorder and other psychiatric disorder group, anxiety group, obsessive compulsive disorder and related group, psychic trauma and stress causation disorder group, dissociation group, somatic symptom and related group, eating behavior disorder and eating disorder group, excretion group, personality disorder group.
  • Patients who will be able to obtain written informed consent.
  • Age of 20 to 80 years.

排除标准

  • Patients who have received rTMS therapy in the past.
  • Patients who presents bvious dementia, depressive state of organic or symptomatic.
  • Patients whose symptoms have improved to the extent that they can be reinstated.
  • Patients who show severe episodes accompanied by psychotic symptoms, impending dilapidation thought or symptoms of tension, and symptoms recommended for electroconvulsive therapy.
  • Patients who have metal indwelling in the cranium or who have a pacemaker implanted in the heart.
  • Patients who have had a history of drug abuse.
  • Patients who have severe mental retardation.
  • Pregnant woman.
  • Patients who was considered ineligible by investigators.

结局指标

主要结局

-

Evaluation of improvement in depressive state by POMS and HAM-D.

次要结局

未报告次要终点

研究者

发起方
未提供

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