跳至主要内容
临床试验/NCT05222113
NCT05222113已完成不适用

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

Bernadette Dian Novita, MD.,PhD1 个研究点 分布在 1 个国家目标入组 87 人开始时间: 2021年8月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
87
试验地点
1
主要终点
Clinical manifestation

研究概览

简要总结

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 January to August 2021

详细描述

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 treatments. Remdesivir and favipiravir are the antivirals recommended by Indonesia's 3rd COVID-19 Management Guidelines. They have a similar mechanism to inhibit virus replication, specifically by inhibiting RNA-dependent RNA polymerase (RdRp) of the virus. Several studies reported that patients who received these antivirals had a lower duration of hospitalization. However, the effectiveness comparison of remdesivir and favipiravir remains unknown.

An observational analytic study using a retrospective cohort design. Eighty-eight medical records of COVID-19 patients from January to August 2021 are collected by consecutive sampling technique, and this research was carried out at Gotong Royong Hospital Surabaya.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 97 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients (eighteen years old or above) with moderate to severe COVID-19 (categorized based on KEPUTUSAN MENTERI KESEHATAN REPUBLIK INDONESIA NOMOR HK.
  • 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

排除标准

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

结局指标

主要结局

Clinical manifestation

时间窗: 2 weeks since drug (remdesivir OR favipiravir) administration

Oxygen needs, cough, dyspnea

次要结局

未报告次要终点

研究者

发起方
Bernadette Dian Novita, MD.,PhD
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Bernadette Dian Novita, MD.,PhD

MD.,PhD

Universitas Katolik Widya Mandala Surabaya

研究点 (1)

Loading locations...

相似试验