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Ivermectin in Treatment of COVID-19

Phase 2
Conditions
COVID
Interventions
Registration Number
NCT04445311
Lead Sponsor
Zagazig University
Brief Summary

confirmed cases with COVID-19 will receive ivermectin as a therapeutic option as well as standard of care treatment and will be compared to those that will receive only standard of care ttt

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria

COVID-19 patients during period of the study more than 18 years old

Exclusion Criteria

refuse to participate pregnancy or lactation hypersensitivity to ivermectin receive any drug with interaction with ivermectin

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Ivermectin groupIvermectingroup that will receive ivermectin plus standard of care ttt
Primary Outcome Measures
NameTimeMethod
time to be symptoms freewithin 21 days after enrollment

duration from day 1 symptoms till 3 days without symptoms

Secondary Outcome Measures
NameTimeMethod
Mechanical ventilationwithin 21 days after enrollement

need mechanical ventilation

hospitalizationwithin 21 days after enrollement

need hospital admission

length of staywithin one month days after enrollement

days spent in hospital

mortalitywithin one month days after enrollement

survived or died

Trial Locations

Locations (1)

Waheed Shouman

🇪🇬

Zagazig, Sharkia, Egypt

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