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Deep Electrical Neuromodulation in Obsessive-compulsive Disorder (NEP-TOC)

2018年7月27日 更新者:University Hospital, Montpellier

Electric Neuromodulation in Refractory Obsessive-compulsive Disorder : the Montpellier Experience (France)

Obsessive-compulsive disorder (OCD) is a neuropsychiatric disease characterised by intrusive, recurrent and persistent thoughts, urges or images (obsessions) and the resulting excessive repetitive behaviours or mental acts according to rigid rules unrealistically aimed at reducing distress (compulsions).

Its lifetime prevalence in the general population is usually estimated between 1 - 3% (Ruscio, Mol Psychiatry, 2010). Despite appropriate pharmacological and cognitive-behavioural treatments, it is commonly estimated that 10% of patients are therapy-refractory and that among improved or recovered patients, sustained efficacy is uncertain.

For treatment refractory OCD patients, a neurosurgical treatment by deep brain stimulation (DBS), has emerged in the late 1990s as a new therapeutic option (Nuttin et al, Lancet, 1999).

The objective of the current study is to report the long-term treatment effects (safety and effectiveness) of DBS from the cohort of six severe and therapy-refractory OCD patients implanted at the French university hospital of Montpellier since 2003.

研究概览

地位

完全的

详细说明

The data needed to carry out the study will be extracted from the medical files of the 6 patients concerned.

The following data will be collected:

  • Age, sex
  • Medical, surgical and psychiatric history
  • History of pharmacological treatments
  • Elements from clinical examination
  • any reported adverse effect
  • scores of the various questionnaires completed throughout the follow-up (including Y-BOCS and GAF)
  • results of biological, morphological, neuropsychological tests
  • Stimulation parameters applied since implantation.

研究类型

观察性的

注册 (实际的)

6

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Montpellier、法国、34295
        • UHMontpellier

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

非概率样本

研究人群

Six patients consisting in three males and three females aged 18 years and over implanted at the University Hospital (CHU) of Montpellier (France) between June 2003 and February 2013.

描述

Inclusion criteria:

  • all patients with severe and refractory OCD according to DSM-IV criteria, confirmed by experienced psychiatrist
  • treated by DBS at the CHU of Montpellier

Exclusion criteria:

- already enrolled in a study protocol at time of implantation

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Yale-Brown Obsessive Compulsive Scale (Y-BOCS)
大体时间:Baseline

10-item scale with scores ranging from 0 to 40; higher scores indicating more severe OCD symptoms.

Patients are defined as responders if they have a score decrease of at least 35% on the Y-BOCS

Baseline
Yale-Brown Obsessive Compulsive Scale (Y-BOCS)
大体时间:12 months

10-item scale with scores ranging from 0 to 40; higher scores indicating more severe OCD symptoms.

Patients are defined as responders if they have a score decrease of at least 35% on the Y-BOCS

12 months

次要结果测量

结果测量
措施说明
大体时间
Global Assessment of Functioning (GAF), axis V of the DSM-IV (APA, 1994).
大体时间:Baseline
a rating scale used to subjectively assess the social and occupational functioning as well as psychological symptoms of adults. The scale ranges from 1 to 100, divided into 10-point intervals describing the level of functioning and symptoms.
Baseline
Global Assessment of Functioning (GAF), axis V of the DSM-IV (APA, 1994).
大体时间:12 months
a rating scale used to subjectively assess the social and occupational functioning as well as psychological symptoms of adults. The scale ranges from 1 to 100, divided into 10-point intervals describing the level of functioning and symptoms.
12 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Fabienne CYPRIEN、University Hospital, Montpellier

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2018年4月1日

初级完成 (实际的)

2018年5月1日

研究完成 (实际的)

2018年6月30日

研究注册日期

首次提交

2018年4月13日

首先提交符合 QC 标准的

2018年7月27日

首次发布 (实际的)

2018年7月30日

研究记录更新

最后更新发布 (实际的)

2018年7月30日

上次提交的符合 QC 标准的更新

2018年7月27日

最后验证

2018年4月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

未定

IPD 计划说明

NC

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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