Overview

Atorvastatin for Reduction of 28-day Mortality in COVID-19: RCT

Status:
Active, not recruiting
Trial end date:
2022-04-01
Target enrollment:
0
Participant gender:
All
Summary
This randomized placebo-controlled double-blinded clinical trial aims to test the efficacy of administering atorvastatin 40 mg to hospitalized COVID-19 patients for 28 days on the all-cause 28-day mortality.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Mansoura University
Treatments:
Atorvastatin
Criteria
Inclusion Criteria:

- We will include adult patients (≥18 years old) with severe and critical COVID19
admitted to the COVID19 Mansoura University isolation hospital. We will include
patients who are PCR-confirmed, clinically or radiologically diagnosed with COVID19.

Cases are defined as severe or critical according to the WHO definition (19); where
critical cases have ARDS, or sepsis, septic shock or pulmonary embolism, acute coronary
syndrome, or acute stroke, while severe cases have the clinical signs of severe pneumonia
and SpO2 <90% on room air, or RR <30 breaths/min without any critical criteria.

Exclusion Criteria:

- chronic statin use, serum creatine kinase (sr CK) > 5 times the upper limit of normal
(ULN), serum transaminases > 5 times ULN, acute hepatic failure, chronic liver disease
(Child-Pugh Classification C), history of rhabdomyolysis or myopathies, severe renal
impairment not receiving renal replacement therapy (estimated Cr cl< 30 ml\min ),
pregnant and lactating women, patients who are expected to die within 48 hours, or
patients on chronic colchicine, cyclosporines, or ritonavir.