IRCT201504053449N18已完成2 期
Comparing efficacy and safety of Valerian and Placebo for prevention of Efavirenz-induced anxiety and depression in HIV positive patients
Vice Chancellor for Research, Tehran University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
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
- 18 years 至 65 years（—）
- 性别
- All
入选标准
- •Patients with confirmed HIV infection, between 18-65 years old, receiving Efavirenz containing antiretroviral treatment.
- •Exclusion criteria:
- •Pregnant and lactating women, previous treatment with Efavirenz, positive history of neuropyschiatric disorders such as severe depression, patients who are receiving mood affecting agents (such as Methadone), positive history of hypersensitivity to herbal products including Valerian, discontinuation of antiretroviral therapy by patient due to any reason, patients who do not tolerate side effects of Valerian (headache, vertigo, stomach pain, nausea, vomiting, diarrhea and palpitation).
排除标准
- 未提供
研究者
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