CTRI/2024/06/068554尚未招募4 期
A real world assessment for Safety and effectiveness of VORtioxeTine and Escitalopram with Clonazepam in anXious depression - VORTEX STUDY
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
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
- •Male or female patients 18 to 65 years with DSM-V defined MDD with anxious
- •depression.
- •Treatment naïve patients or known cases already on VOR or ESC not exceeding two weeks of active treatment.
- •? Patients with MADRS score is greater than 20 and HAM-A score is greater than 25.
- •Patient with normal physical examination clinical laboratory and ECG findings (as per
- •physicians discretion)
- •Patients who are willing to sign the informed consent form
排除标准
- •Patient aged less than 18 years and more than 65 years will be excluded.
- •Patient with MADRS less than 19 and HAM-A less than 24.
- •Patients requiring second generation antipsychotics or lithium.
- •Patient in which the use of benzodiazepine is contraindicated.
- •Patient with other conditions who do not fit into the criteria of the study as per the
- •Patient with known hypersensitivity to Vortioxetine, Escitalopram, Clonazepam or any
- •excipients.
- •Patients who are not willing to sign the informed consent form
研究者
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