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The effect of naproxen on the healing process of patients with COVID-19

Phase 3
Completed
Conditions
corona virus disease.
COVID-19, virus not identified
U07.2
Registration Number
IRCT20200324046850N3
Lead Sponsor
Abadan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
80
Inclusion Criteria

COVID-19 patients that have positive PCR test of nasopharyngeal sample or have positive CT Scan
Having consent to participate in the intervention

Exclusion Criteria

pregnant or breast feeding women
Those taking losartan and captopril.
Those with a history of intestinal ulcers or gastrointestinal bleeding.
Children under 14 years

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to clinical improvement defined as start of taking medication time to the next 28 days. Timepoint: The beginning of the study ,the seventh day, the fourteenth day, the twenty-first day, the twenty-eighth day. Method of measurement: Medical record.
Secondary Outcome Measures
NameTimeMethod
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