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临床试验/IRCT20110918007582N2
IRCT20110918007582N2招募中3 期

Comparison of the efficacy of adding clonidine to SSRI and treating patients with SSRI alone in patients with treatment-resistant obsessive compulsive disorder

Esfahan University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
no limit 至 no limit(—)
性别
All

入选标准

  • The presence of obsessive-compulsive disorder criteria based on DSM-V-TR
  • Receive at least 12 weeks with a maximum dose of a serotonergic drug (SSRI or Clomipramine)
  • Moderate to severe symptoms based on the obsessive-compulsive- Yerobyll-Brown scale (YBOCS) with a score of more than 16
  • Obtain informed consent from the patient
  • No initial diagnosis of psychiatric disorders and mood disorder (bipolar or MDD)
  • Absence of drug use or dependence
  • There is no uncontrolled physical illness (such as diabetes, blood pressure, etc.)
  • There is no previous history of Clonidine use
  • Lack of pregnancy and lactation or planning for pregnancy during the study
  • There is no seizure disorder
  • No suicide attempt
  • Not taking beta-blocker
  • Failure to receive synchronous psychological intervention

排除标准

  • Cancellation of participation in the study at each stage of the research
  • Pregnancy at each stage of the research

研究者

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