CTRI/2024/04/066458尚未招募4 期
A comparative study to assess the efficacy and safety of Vortioxetine versus sertraline in patients suffering from Anxiety Disorder - NI
Mitsha Nagpal0 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
- 4 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
- •1. Both male and female patients aged between 18 and 60 years.
- •2. Those giving written consent/guardians giving written consent (in cases where the patients were too ill to understand the process of informed consent and give an informed choice.)
- •3. People diagnosed with anxiety disorder as per ICD-10 diagnostic criteria.
- •4. HAM-A score =18
排除标准
- •1. Systemic or Neurological Disorder affecting Cognition, Behavior or Mental Status.
- •2. Substance dependence except for Nicotine and Caffeine within the past month of entering the study.
- •3. Long-standing medical or surgical illnesses.
- •4. Patients with mental retardation or organic brain disorders.
- •5. Patients suffering from neurological, metabolic and vascular conditions affecting sexual function.
研究者
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