IRCT20190810044500N5已完成3 期
Investigation of the efficacy and safety of colchicine In combination with standard treatment on covid-19 patients: A clinical trial
Yazd University of Medical Sciences0 个研究点目标入组 200 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
- 200
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 70 years(—)
- 性别
- All
入选标准
- •Age 18 to 70 years
- •- Detection of COVID-19 in the last 24 to 48 hours
- •- Candidate for hospitalization (o2sat <93% or RR> 24 or Pao2 / Fio2 <300)
- •- COVID-19 patients hospitalized with hospital indications according to the guideline of the country that has pulmonary infiltration in CT scan
- •-Not being pregnant and not becoming pregnant until 30 days after the end of the study
- •- No consumption of colchicine during the last week ( due to the half-life of 20-40 hours of the drug)
- •- Outpatients with pulmonary infiltration on CT scan
排除标准
- •Patients with a history of Crohn or Ulcerative colitis, diarrhea, or chronic malabsorption
- •Neuromuscular diseases
- •GFR less than 30 ml per minute
- •History of cirrhosis, hepatitis and severe liver disease
- •Patients receiving chemotherapy for cancer
- •Patients currently taking colchicine for other uses, such as gout or Mediterranean fever
- •Patients with a history of allergic reactions or allergies to colchicine
- •Pregnancy and lactation
研究者
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