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临床试验/NCT00830921
NCT00830921
终止
不适用

A Randomised Crossover Study to Investigate the Effect of Transcranial Magnetic Stimulation of the Anterior Cingulate Cortex on "Air Hunger"

University of Oxford1 个研究点 分布在 1 个国家目标入组 12 人2008年2月
适应症Malignancy

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Malignancy
发起方
University of Oxford
入组人数
12
试验地点
1
状态
终止
最后更新
13年前

概览

简要总结

The treatment we are studying is Transcranial Magnetic Stimulation (TMS). In TMS, an electromagnetic pulse is passed into the brain through a coil placed on the head. Previous studies have shown TMS to be capable of altering brain activity in specific areas; for example it has been used to improve mood in clinical depression. In this study we will assess if, by targeting TMS to the brain area responsible for feeling breathless, participants' breathlessness will be improved

详细描述

This protocol describes an exploratory crossover pilot study to assess whether targeted repetitive pulse Transcranial Magnetic Stimulation (TMS) i.e. targeted at the anterior cingulate cortex (ACC), affords relief of 'air hunger' in patients with breathlessness refractory to maximal medical therapy, compared to 'control' TMS directed at a remote site independent of the area of interest (within the lateral right parietal region of the brain). 12 right-handed patients suffering from refractory dyspnoea will receive pulses of targeted TMS or control TMS (crossover design), in a random order. The order will be random and use a minimisation procedure for baseline dyspnoea severity and sex. Repetitive targeted TMS (or control) pulses at 110% motor threshold at a frequency of 1Hz will be given for a 15 minute period1. On a second, later, day the same subjects will perform the same protocol after receiving inhaled menthol or control (normal, non odorous air), in random order. Outcomes will be assessed during the 10 minutes after targeted TMS/control TMS during which post stimulation inhibition of neural activity is expected.

注册库
clinicaltrials.gov
开始日期
2008年2月
结束日期
2012年1月
最后更新
13年前
研究类型
Observational
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Refractory dyspnoea (persisting sensation of air hunger despite optimisation of medical treatment)
  • Histocytologically proven thoracic malignancy
  • Written informed consent

排除标准

  • Age \<18 years
  • Left-handed
  • Structural brain disease (including cerebral metastasis)
  • Personal or family history of seizures
  • Implantable metallic objects e.g. a pacemaker, or other contraindication to transcranial magnetic stimulation
  • Pregnant or breast feeding
  • Previous electroconvulsive therapy (ECT)
  • Poor mobility
  • Visual impairment
  • Lack of social support / home to go to after the study treatment

结局指标

主要结局

未指定

研究点 (1)

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