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Effect of Atorvastatin in the management of COVID-19

Evaluation of the efficacy of Atorvastatin in the management of critically ill COVID-19 patients: A Randomized-controlled clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150221021159N7
Enrollment
60
Registered
2021-11-10
Start date
2021-10-23
Completion date
Unknown
Last updated
2021-11-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19. Coronavirus infection, unspecified

Interventions

Intervention 1: Intervention group: In addition to the essential and standard treatment for COVID-19, one tablet of atorvastatin 20 mg (Abidi pharmaceutical company), once daily will be administered f

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age 18 years or older Diagnosis of COVID-19 by RT PCR test and CT scan of the lung and the opinion of the specialist physician Hospitalization in the intensive care unit Full consent and acceptance of the patient or their legal guardian to recruit in the study Possibility to follow the patient for at least 7 days

Exclusion criteria

Exclusion criteria: Contraindications to the use of atorvastatin include allergic reactions to the drug, active liver disease or persistent and unexplained increase in liver enzymes, pregnancy and lactation, severe hepatic or renal insufficiency (clcr <30 ml / min) Malignancy or underlying immunodeficiency or concomitant use of immunosuppressive drugs Intubated patient under care with mechanical ventilation

Design outcomes

Primary

MeasureTime frame
Clinical improvement of COVID-19. Timepoint: Day: 1, 3, 7 and 14. Method of measurement: APACHE score, evaluation of vital signs? relevant laboratory and arterial blood gas analysis.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadi Farsaei

Esfahan University of Medical Sciences

Farsaei@pharm.mui.ac.ir+98 31 3792 7071

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026