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Evaluation of atorvastatin tablet as an adjuvant treatment for patients with mild to moderate COVID-19 in Qaem Hospital, Mashhad

Phase 2
Recruiting
Conditions
COVID-19 pneumonia.
COVID-19, virus identified
U07.1
Registration Number
IRCT20200408046990N3
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

Laboratory or clinical diagnosis of COVID-19 with admission indication
age between 18-65 y
sign of the written consent
not concomitant use of kaletra or other PIs, cyclosporine, colchicine, ciproterone, danazol, gemfibrozil, potent CYP3A4 inhibitors or inducers like macrolides, CCBs, Azoles, rifampin, phenytoin
not using statin before including in the study

Exclusion Criteria

history of allergy to statins
pregnancy and lactation
active liver disease or rise of LFT during study
including in other studies
start of PIs
ADR occurrence e.g. rhabdomyolysis
severe renal failure (GFR<30 ml/min)
indication for intubation or ICU
not being able to swallow medication

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fever. Timepoint: daily. Method of measurement: thermometer.;Clinical response to treatment (including improvement of cough, myalgia, headache, Olfactory and taste disorders). Timepoint: daily. Method of measurement: based on patients examination and interview.;Radiologic response. Timepoint: two weeks after treatment. Method of measurement: lung CT scan.;Laboratory response. Timepoint: weekly. Method of measurement: assessment of serum level of CRP and CBC diff.;Drug adverse reaction. Timepoint: daily. Method of measurement: patient file and interview.
Secondary Outcome Measures
NameTimeMethod
Duration of hospitalization. Timepoint: end of the treatment. Method of measurement: patients' file.;Patients' clinical outcome. Timepoint: at the of the treatment. Method of measurement: patients' file.
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