IRCT20080901001165N60招募中3 期
Investigating the efficacy of Provita Capsule in controlling the symptoms of patients with COVID-19
Bagheiat-allah University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 30
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
- •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 either lung CT-Scan result, which is typical for COVID-19 pulmonary involvement,or RT-PCR confirmation.
- •Less than 7 days have passed since the onset of symptoms.
排除标准
- •History of allergy to the ingredients;
- •The patient is in another clinical trial at the same time;
- •The patient needs to receive medical care from the intensive care unit;
- •Impossibility of oral nutrition;
研究者
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