rTMS Bimodal Treatment For Patients With Subjective Idiopathic Tinnitus: A Pilot Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 5
- 试验地点
- 2
- 主要终点
- Adverse Events
研究概览
简要总结
Repetitive Transcranial Magnetic Stimulation (rTMS) is a novel brain stimulation technique that uses pulsating magnetic fields to stimulate underlying neurons in the cerebral cortex. The investigators propose an open-label pilot study investigating the effectiveness of rTMS in the treatment of tinnitus stimulation of the left dorsolateral prefrontal cortex (DLPFC), an area known to be important for mood and attention, along with stimulation of the left temporoparietal cortex (TPC). This is a feasibility pilot study.
详细描述
Converging data implicate structures of the brain that are important for mood and attention as playing a role in the maintenance of tinnitus; suggesting an alternative rTMS treatment approach that targets these structures. A growing number of studies demonstrate involvement of the prefrontal cortex in the generation and maintenance of tinnitus. rTMS stimulation in the dorsolateral prefrontal cortex in association with stimulation in the temporoparietal cortex has been shown to increase the durability of the TPC stimulation. The independent effect of rTMS stimulation to the DLPFC is not known. Studies in depression suggest that increasing the intensity and duration of stimulation has beneficial treatment effects. However, the field is new and more work is needed to assess the effectiveness of this treatment, predictors and correlates of response, and safety.
Recent exciting work in schizophrenia used a bimodal (DLPFC and TPC) treatment approach in pharmacologically non-responsive patients. The study used high-frequency stimulation to the left DLPFC and low-frequency stimulation to the left TPC. Bimodal rTMS stimulation of left DLPFC and left TPC induced clinical improvement in pharmacologically non-responsive schizophrenia patients and may have improved their short-term verbal memories.57
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Must be between the ages of 18 and 60 years.
- •Subjective, idiopathic, troublesome, unilateral or bilateral, non-pulsatile tinnitus of ≥ 2 month's duration but no greater than 5 year's duration.
- •Bothersome Tinnitus according to Tinnitus Handicap Inventory score.
- •Must be able to understand, speak, read and write English proficiently
- •Able to provide informed consent
- •Women who are of childbearing potential must agree to use a medically acceptable form of birth control and must have a negative urine pregnancy test at screening
排除标准
- ••• Patients with tinnitus related to cochlear implantation, retrocochlear lesion, or other known anatomic/structural lesions of the ear and temporal bone. Patients with a history of stapedectomy and insertion of implant will be excluded.
- •Hypersensitive to noises (hyperacusis)
- •Patients with history of head injury with 15 minutes or more loss of consciousness or required medical treatment.
- •Patients with cardiac pacemakers; intracardiac lines; implanted medication pumps; implanted electrodes in the brain; other implanted electrical or magnetic medical devices; or other intracranial metal objects or shrapnel, with the exception of dental fillings.
- •Patients with additional significant neurological disorders including increased intracranial pressure, brain mass, epileptic seizures (or family history of epileptic seizures), history of stroke, transient ischemic attack within 2 years, cerebral aneurysm, Huntington's chorea or multiple sclerosis.
- •Patients with an acute or unstable medical condition including all patients with any significant heart disease, pneumonia, uncontrolled hypertension, or other disorders which would require stabilization prior to initiation of transcranial magnetic stimulation.
- •Active alcohol and/or drug dependence or history of alcohol and/or drug dependence within the last year.
- •Patients with moderate to severe clinical depression as evidenced by a score of 15 or greater on the PHQ-
- •Patients who, in the opinion of the psychiatric sub-investigator, demonstrate moderate to severe depressive symptoms according to DSM-IV-TR criteria for Major Depressive Disorder.
- •Patients with psychiatric illness or trauma which would prohibit participation in the study.
- •Patients with active psychotic symptoms or a history of psychotic disorder
- •Female patients of child-bearing potential, unless sterilized or using an appropriate form of birth control acceptable to the research team.
- •Currently breastfeeding
- •Currently pregnant
- •Patients will be excluded if a motor threshold cannot be elicited,
- •Patients whose ability to give informed consent is in question
- •Undiagnosed symptomatic hypertension: .
- •Undiagnosed asymptomatic hypertension:
- •Any patient who has scheduled an elective surgery or change in medication during the 5 weeks of the study.
- •Use of Neuromonics Device during duration of study or currently in Tinnitus Retraining Program during course of study.
- •Any medical condition that, in the opinion of the investigators, confounds study results or places the subject at greater risk.
- •Patients currently taking psychotropic medications including antidepressants, benzodiazepines, anticonvulsants, stimulants, antipsychotics, or anxiolytics.
- •Tinnitus related to a Workman's Compensation claim or litigation-related event that is still pending.
结局指标
主要结局
Adverse Events
时间窗: Daily for 2 weeks.
Subject will be queried for Adverse Events daily for 2 weeks of treatment. This is foremost a feasibility study, so measure of Adverse Events and relation to treatment is primary outcome.
次要结局
- Change in Tinnitus Handicap Inventory(Baseline, 2 weeks)
研究者
Jay F. Piccirillo, MD
Professor, Director of Clinical Outcomes
Washington University School of Medicine