CTRI/2021/07/034827招募中2 期
High dose statin for mild/moderate COVID-19 patients: A pragmatic parallel-group open-label randomized trial with blinded endpoint assessment - COVI-TI
MRU RIMS Ranchi0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
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
入选标准
- •1.Diagnosed case of COVID-19 based on RT-PCR or typical CT chest findings.
- •Mild COVID-19: Individuals who test positive for SARS-CoV-2 using a virologic test (i.e., a nucleic acid amplification test [NAAT] or an antigen test) and who have any of the various upper respiratory tract symptoms (e.g., cough, sore throat, malaise, headache, muscle pain, nausea, vomiting, diarrhea, loss of taste and smell) with or without fever but who do not have shortness of breath or hypoxia. Sp02 on room air more than 93%.
- •Moderate COVID-19: Individuals who test positive for SARS-CoV-2 using a virologic test (i.e., a nucleic acid amplification test [NAAT] or an antigen test), who show evidence of lower respiratory disease during clinical assessment or imaging, and who have an oxygen saturation (SpO2) 90 ââ?¬â?? 93% on room air at sea level or respiratory rate of 24-30 per minute.
- •2. Presentation within 7 days of onset of fever.
- •3. Age 18 to 75 years
- •4. Statin naÃ?¯ve patients (should not use statin for regular 15 days in last one year)
- •5. Previously documented statin intolerance
- •6.Unable to provide written informed consent form
排除标准
- •1.Age < 18 years
- •2.Severe COVID-19 pneumonia: Individuals who test positive for SARS-CoV-2 using a virologic test (i.e., a nucleic acid amplification test [NAAT] or an antigen test), who show evidence of lower respiratory disease during clinical assessment or imaging and who have SpO2 <90% on room air at sea level or respiratory frequency >30 breaths/min
- •3.Patients already on statins for dyslipidemia or cardiovascular disorders
- •4.Hypersensitivity to statins.
- •5.Active liver disease or unexplained persistent elevations of serum transaminases exceeding 2.5 times
- •6.Pregnancy and lactating mothers.
- •7.Concomitant treatment with the immunosuppressant cyclosporine or hepatitis C antivirals glecaprevir/pibrentasvir/tipranavir/ritonavir.
研究者
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