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Dataset Information

Multicenter, single-blind, randomized controlled study of the efficacy and safety of favipiravir and nafamostat mesilate in patients with COVID-19 pneumonia.


ABSTRACT:

Objectives

To evaluate the efficacy and safety of nafamostat combined with favipiravir for the treatment of COVID-19.

Methods

We conducted a multicenter, randomized, single-blind, placebo-controlled, parallel assignment study in hospitalized patients with mild-to-moderate COVID-19 pneumonia. Patients were randomly assigned to receive favipiravir alone (n = 24) or nafamostat with favipiravir (n = 21). The outcomes included changes in the World Health Organization clinical progression scale score, time to improvement in body temperature, and improvement in oxygen saturation (SpO2).

Results

There was no significant difference in the changes in the clinical progression scale between nafamostat with favipiravir and favipiravir alone groups (median, -0.444 vs -0.

SUBMITTER: Ikeda M 

PROVIDER: S-EPMC9810545 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature