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临床试验/IRCT20201024049134N4
IRCT20201024049134N4尚未招募2 期

The Efficacy of standard treatment and dimethyl fumarate in the treatment of patients with COVID-19

Babol University of Medical Sciences0 个研究点目标入组 30 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
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 no limit(—)
性别
All

入选标准

  • Men and women of at least 18 years of age capable of providing informed consent
  • Confirmation of COVID-19 with RT-PCR
  • Need for hospitalization
  • No need for mechanical ventilation
  • No need to more than 10 L/min of supplemental oxygen by any device.
  • The patient must meet at least one of the following high-risk criteria: age 70 years or older, obesity (BMI = 30 kg/m2), diabetes mellitus, uncontrolled blood pressure (systolic blood pressure> 150 mm Hg), history of respiratory disease (Including asthma or COPD), history of heart failure, history of coronary artery disease, fever > 38.4°C in the last 48 hours, shortness of breath at the time of referral, Bicytopenia, Pancytopenia, or a combination of neutrophilia and lymphopenia

排除标准

  • History of allergy to dimethyl fumarate
  • Use of dimethyl fumarate before current hospitalization
  • Patients more than 70 years of age with a history of any of the following in the last six months: Class III / IV Heart Failure Based on the New York Heart Association (NYHA) classification, Insulin-dependent diabetes, Angina pectoris, Malignancy
  • Uncontrolled bacterial, fungal, or viral infection (other than COVID-19).
  • Any history of receiving convalescent plasma therapy
  • Absolute neutrophil count (ANC) < 500
  • Platelets count < 50,000
  • Pregnant women or those intending to become pregnant
  • Breastfeeding women
  • AST or ALT > 5 times the upper limits of normal (ULN)
  • Estimated glomerular filtration rate (eGFR) < 30 ml/min in 1.73 m2 using MDRD equation

研究者

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