IRCT20180712040449N2招募中3 期
Formulation and evaluation of their efficacy of herbal capsule and decoction in patients with COVID-19 via a randomized clinical trial.
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 68
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 75 years（—）
- 性别
- All
入选标准
- •Patients with one or more of the following symptoms in addition to acute respiratory disease (ARI):• RR> 30• PO2 <93%• Pulmonary infiltration in chest x-ray• Clinical judgment of a specialist
- •Age range of 18 to 75 years in both genders
- •Lack of any serious concomitant disease of the heart, brain, or lungs, metabolic disorders, and etc.
- •The patient’s ability and own will to fill out a personal consent form for inclusion in the study
- •Patient not intubated.
排除标准
- •Pregnancy and lactation
- •Any history of allergy to any of the herbal product components
- •Inability to take a drug per-oral
- •Any condition that precludes continuance of medical intervention based on the judgment of a physician.
- •Need for intubation
- •Nausea and vomiting and oral intolerance
- •Resistant hypoxemia
- •Reduced level of consciousness
- •Hemodynamic instability
- •Hypercapnia - respiratory fatigue
- •Any manifestation of known side effects of any of the herbal product components
研究者
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