IRCT20080901001165N59已完成3 期
Investigating the efficacy and safety of Nivasha oral spray in controlling the symptoms of patients with COVID-19
anoalvand arad company0 个研究点目标入组 80 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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 no limit（—）
- 性别
- All
入选标准
- •Age: equal or more than 18 years;
- •The patient have written consciously and freely consent to participate in the study.
- •The patient's clinical symptoms (dry cough, shortness of breath, fever) confirm COVID-19.
- •Confirmed diagnosis of COVID-19, with RT-PCR confirmation.
- •Less than 7 days have passed since the onset of symptoms.
排除标准
- •History of allergy to this spray ingredients;
- •The patient is in another clinical trial at the same time;
- •The patient needs to be hospitalized;
研究者
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