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Effectiveness of favipiravir in comparison with Tenofovir Alafenamid in patients with COVID-19

Phase 2
Recruiting
Conditions
COVID-19.
COVID-19
U07.1
Registration Number
IRCT20150808023559N23
Lead Sponsor
Ardabil University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Diagnosis of COVID-19 based on chest CT scan or positive PCR test for COVID-19
Requiring hospitalization
Patient's age between 16 and 100 years
Signing informed consent form

Exclusion Criteria

Receiving other antiviral medicationsrenal failure
Pregnancy
HIV
Lactation
Renal failure

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hospital mortality. Timepoint: Up to two weeks after the intervention on a daily basis. Method of measurement: Patient medical records.
Secondary Outcome Measures
NameTimeMethod
Duration of hospitalization. Timepoint: From the time of hospitalization to the patient's discharge from the hospital. Method of measurement: Patient medical records.
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