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临床试验/CTRI/2023/12/060748
CTRI/2023/12/060748尚未招募2 期

Efficacy and safety profile of Vortioxetine as an add-on molecule in Obsessive-Compulsive Disorder; A Randomized Double-Blinded Placebo-Controlled Superiority Trial - Not applicable

Indican Council of Medical Research0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

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

入选标准

  • i. Patients diagnosed with OCD as per ICD 11 by a psychiatrist
  • ii. OCD rated as moderate to severe (YBOCS score 16+)
  • iii. Patients who are drug naïve or have not taken any SRIs for the last 7 days at least.

排除标准

  • i. Patients with psychotic symptoms
  • ii. Patients with co-morbid major psychiatric illness
  • iii. Patients with comorbid substance use disorder in dependence pattern except tobacco
  • and caffeine.
  • iv. Pregnant and lactating mothers.
  • v. Patients with co-morbid medical or neurological illness
  • vi. Patients with history of adverse drug reaction to Vortioxetine in the past

研究者

发起方
Indican Council of Medical Research

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