Status:

COMPLETED

OBSERVATIONAL STUDY OF COMPARISON EFFECTIVITY BETWEEN REMDESIVIR AND FAVIPIRAVIR IN SURABAYA, INDONESIA

Lead Sponsor:

Bernadette Dian Novita, MD.,PhD

Conditions:

Duration of Hospitalization

Clinical Manifestation of COVID-19

Eligibility:

All Genders

18-97 years

Brief Summary

In order to compare the effectiveness between Remdesivir and Favipiravir, an observational analytic study using a retrospective cohort design. Eighty-eight medical records of COVID-19 patients from Ja...

Detailed Description

Coronavirus Disease 2019 (COVID-19) is an infectious disease caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2). Antiviral therapies are considered to be one of the COVID-19 treatm...

Eligibility Criteria

Inclusion

  • Adult patients (eighteen years old or above) with moderate to severe COVID-19 (categorized based on KEPUTUSAN MENTERI KESEHATAN REPUBLIK INDONESIA NOMOR HK. 01. 07/MENKES/413/2020);
  • Admitted to Gotong Royong Hospital Surabaya from January 2021 to August 2021;
  • Received remdesivir OR favipiravir with minimal five days of treatment
  • Not in pregnancy and lactating condition

Exclusion

  • female patient with pregnancy and lactation
  • patient whom was passed away or forced home during two-weeks observation period

Key Trial Info

Start Date :

August 1 2021

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

September 25 2021

Estimated Enrollment :

87 Patients enrolled

Trial Details

Trial ID

NCT05222113

Start Date

August 1 2021

End Date

September 25 2021

Last Update

February 3 2022

Active Locations (1)

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Gotong Royong Surabaya Hospital

Surabaya, East Java, Indonesia, 60119