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临床试验/NCT00577070
NCT00577070已完成2 期

Evaluation of the H-Coil Transcranial Magnetic Stimulation(TMS) Device- Augmentation for Drug Resistant Depression

BeerYaakov Mental Health Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2008年1月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40
试验地点
2
主要终点
Treatment response defined as at least a 50% decrease in Hamilton Depression Rating Scale (HAM-D24). Remission is defined as below 8 in Hamilton Depression Rating Scale (HAM-D24)

研究概览

简要总结

There is a general consensus of efficacy of TMS in treatment of major depression,yet results are not satisfying.A new coil ("H"-coil, recently invented in Weizmann Institute of Science, Neurobiology Department, Rehovot, Israel) is supposed to be capable of stimulating deeper brain structures than conventional coils.TMS using this coil was named by its developers as "deep TMS" and will hence be refered to by this name.

So far, deep TMS have studied in Israel with promising sucssess in patients with Major depression (An on-going study).A safety study with good results have been recently published.The aim of this study is to reinforce initial results in major depression using deep TMS.

详细描述

A group of 40 patients with major depression will be randomly assigned to deep TMS with H-1 coil in frequency of 20 HZ or H-2 coil in frequency of 0.1 HZ with 120% of motor threshold to the prefrontal cortex . No change in anti-depressant medication one month prior to study is a prerequisite.Deep TMS will be administered for 4 weeks.During TMS exposure subjects will be exposed to a conversation in which they talk about their depression and their ruminations.Patients will be evaluated using Hamilton Depression Rating Scale (HAM-D24),Hamilton Anxiety Rating Scale (HAM-A),Clinical Global Impression - Improvement(CGI-I) ,Beck Depression Inventory (BDI),Visual Analog Scale (VAS).

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
Double (Participant, Investigator)

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

入选标准

  • Right handed ,18-65 year old male or female subjects
  • Diagnosed according to DSM-V-TR as suffering from Major depression using SCID interview
  • Score of 22 or more in the Hamilton Depression Rating Scale (HAM-D24)
  • The present depressive episode have been treated with at least 2 different anti-depressive drugs at peak doses for at least 6 weeks with not more than a partial response.Augmentation strategies may be included.

排除标准

  • Cardiac pacemaker implant, or a history of epilepsy, neurosurgery, or brain trauma patients suffering from chronic medical conditions of any sort:
  • History of current hypertension
  • History of seizure or heat convulsion
  • History of epilepsy or seizure in first degree relatives
  • History of head injury
  • History of any metal in the head (outside the mouth)
  • Known history of any metallic particles in the eye
  • Implanted cardiac pacemaker or any intra-cardiac lines
  • Implanted neuro-stimulators
  • Surgical clips or any medical pumps
  • History of frequent or severe headaches
  • History of migraine
  • History of hearing loss
  • Known history of cochlear implants
  • History of drug abuse or alcoholism
  • Pregnancy or not using a reliable method of birth control (non-pregnancy will be proved by beta-HCG test)
  • Systemic and metabolic disorders
  • Inadequate communication skills or under custodial care.

结局指标

主要结局

Treatment response defined as at least a 50% decrease in Hamilton Depression Rating Scale (HAM-D24). Remission is defined as below 8 in Hamilton Depression Rating Scale (HAM-D24)

时间窗: 2 months

次要结局

未报告次要终点

研究者

发起方
BeerYaakov Mental Health Center
申办方类型
Other Gov

研究点 (2)

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