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临床试验/NCT01589315
NCT01589315已完成2 期

Focal Electrical Administered Seizure Therapy (FEAST) for Major Depression

Medical University of South Carolina2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2007年1月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
17
试验地点
2
主要终点
Remission Based on HDRS, Hamilton Depression Rating Scale, 24 Item.

研究概览

简要总结

This pilot, open label investigation evaluates the safety and efficacy of a new form of electroconvulsive therapy (ECT). Both the efficacy and adverse cognitive effects of ECT are highly contingent on the intracerebral current paths and current density of the ECT stimulus. However, the impedance of the skull and individual differences in skull anatomy severely limit the spatial targeting of stimulation, and create marked individual differences in intracerebral current density. To address these problems, the investigators are exploring various means of overcoming this limitation.

An approach is to modify the electrical stimulus to induce focal seizures. The most common methods of ECT administration in the US use a bidirectional, constant current, brief pulse, with large (approximately 3 sq. in. surface area) and identically sized and shaped electrodes. In contrast, in this protocol the investigators have coupled unidirectional current flow with an electrode geometry involving a small and large electrode that differ by more than 3:1 in surface area.

Unidirectional currents were widely used in ECT during the, 1940's and continue to be used in European and American devices today. Transcranial electrical stimulation can be made focal by stimulating with an anode-cathode arrangement, with the electrodes differing in surface area. The investigators have shown in nonhuman primates the capacity to produce focal frontal seizure induction under conditions when a unidirectional current flows from a small anterior anode (placed on the forehead over the nasion) to a large posterior cathode just anterior to the motor strip. Furthermore, the investigators expect that some, if not all, of these seizures do not result in motor convulsions.

Thirty outpatients referred for ECT will participate. Relative to concurrent reference data from our ongoing ECT protocols, the investigators hypothesize that acute and subacute adverse cognitive effects of FEAST will be substantially less than those in patients receiving state-of-the art ECT, but with a traditional bidirectional, nonfocal stimulus. The investigators also hypothesize that the majority of patients will remit with FEAST. Thus, by improving the efficiency of the ECT stimulus with the switch to unidirectional current and the use of a new electrode geometry, the investigators expect to be able to induce focal seizures. The investigators hypothesize that this pilot study will provide evidence that this treatment is superior to traditional ECT in having lower dosing requirements and a superior side effect profile.

详细描述

This study will provide preliminary evaluation of the following:

  1. Determination of whether focal seizures can be induced with the FEAST methodology (unidirectional stimulation, small anterior and large posterior electrode).

  2. Focality will be assessed by the occurrence of non-motor seizures.

  3. Electroencephalographic evidence of pronounced asymmetry in frontal leads.

  4. Determination of whether the FEAST methodology results in reduced seizure threshold.

a. Seizure threshold will be quantified at the start of the treatment course using the standard method of limits titration procedure and compared to threshold determinations in matched patients who were treated with conventional ECT methods. 3. Characterization of dynamic impedance using the FEAST methodology.

a. Dynamic impedance during the passage of the electrical stimulus will be quantified during each administration and compared to the values obtained in matched patients who were treated with conventional ECT methods. 4. Characterization of the efficacy of the FEAST methods and the safety of the treatment.

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 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 90 years (inclusive)
  • Diagnosis of major depressive disorder
  • Pretreatment HRSD score ≥ 18
  • ECT indicated
  • Willing and capable of providing informed consent

排除标准

  • History of schizophrenia,
  • schizoaffective disorder,
  • other functional psychosis, or
  • rapid cycling bipolar disorder
  • History of neurological illness or insult other than conditions associated with psychotropic exposure (e.g., tardive dyskinesia)
  • Alcohol or substance abuse or dependence in the past year (RDC)
  • Secondary diagnosis of a delirium, dementia, or amnestic disorder (DSM-IV), pregnancy, or epilepsy
  • Requires especially rapid antidepressant response due to suicidality, psychosis, inanition, psychosocial obligations, etc.
  • Unable to tolerate psychotropic washout and no psychotropic medication during the ECT trial, other than lorazepam (up to 3 mg/d PRN)
  • ECT in the past six months

研究组 & 干预措施

FEAST

Experimental

Active right unilateral focal ECT

干预措施: focal ECT (Device)

结局指标

主要结局

Remission Based on HDRS, Hamilton Depression Rating Scale, 24 Item.

时间窗: up to 4 weeks

The number of treatment sessions is not fixed and could extend up to 12 provided that patients show continued improvement and tolerate the treatment. With 3 FEAST sessions per week, the course may take up to 12 weeks to be completed. The Hamilton Rating Scale for Depression is a widely used clinician administered rating.Scores range from (Min) 0 to (Max) 52. Higher score means worse depression. The definition of remission was a Ham Depression Score (24 item) of \< or equal to 10.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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