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Efficacy of Faviprevir in COVID-19 Treatment

Phase 2
Completed
Conditions
COVID
Interventions
Registration Number
NCT04351295
Lead Sponsor
Tanta University
Brief Summary

Faviprevir in COVID-19 treatment

Detailed Description

Clinical Study Evaluating the Efficacy of Faviprevir in COVID-19 treatment

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
92
Inclusion Criteria
  • Patients with covid 19
Exclusion Criteria
  • Allergy or contraindications to faviprevir

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
FaviprevirFavipiravirFaviprevir
chloroquineChloroquinechloroquine
Primary Outcome Measures
NameTimeMethod
Number of patients with mortality or need for mechanical ventilation6 months

Number of patients with mortality or need for mechanical ventilation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Tanta University, Ainshams University

🇪🇬

Tanta, Egypt

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