Effectiveness of glucocorticoid therapy in patients with severe novel coronavirus pneumonia: protocol of a randomized controlled trial
10.3760/cma.j.issn.0366-6999.2020.0020
- Author:
Yi-Hong ZHOU
1
;
Yuan-Yuan QIN
2
;
Yan-Qiu LU
1
;
Feng SUN
2
;
Sen YANG
2
;
Vijay HARYPURSAT
2
;
Sheng-Quan TANG
2
;
Yin-Qiu HUANG
2
;
Xiao-Qing HE
1
;
Yan-Ming ZENG
1
;
Yao LI
2
;
Xiao-Lei XU
1
;
Ting ZHAO
2
;
Yao-Kai CHEN
1
Author Information
1. Division of Infectious Diseases, Chongqing Public Health Medical Center, Chongqing 400036, China
2. Science and Education Division, Chongqing Public Health Medical Center, Chongqing 400036, China
- Publication Type:Journal Article
- Keywords:
2019-nCoV;
COVID-19;
glucocorticoids;
severe pneumonia;
ARDS
- From:
Chinese Medical Journal
2020;133(0):E020-E020
- CountryChina
- Language:English
-
Abstract:
Background:At the end of 2019, a novel coronavirus outbreak emerged in Wuhan, China, and its causative organism has been subsequently designated the 2019 novel coronavirus (2019-nCoV). The virus has since rapidly spread to all provinces and autonomous regions of China, and to countries outside of China. Patients who become infected with 2019-nCoV may initially develop mild upper respiratory tract symptoms. However, a significant fraction of these patients goes on to subsequently develop serious lower respiratory disease. The effectiveness of adjunctive glucocorticoid therapy uses in the management of 2019-nCoV infected patients with severe lower respiratory tract infections is not clear, and warrants further investigation.
Methods:The present study will be conducted as an open-labelled, randomised controlled trial. We will enrol 48 subjects from Chongqing Public Health Medical Center. Each eligible subject will be assigned to an intervention group (methylprednisolone via intravenous injection at a dose of 1-2mg/kg/day for 3 days) or a control group (no glucocorticoid use) randomly, at a 1:1 ratio. Subjects in both groups will be invited for 28 days of follow-up which will be scheduled at 4 consecutive visit points. We will use the clinical improvement rate as our primary endpoint. Secondary endpoints include the timing of clinical improvement after intervention, duration of mechanical ventilation, duration of hospitalization, overall incidence of adverse events, as well as rate of adverse events at each visit, and mortality at 2 and 4 weeks.
Discussion:The present coronavirus outbreak is the third serious global coronavirus outbreak in the past two decades. Oral and parenteral glucocorticoids have been used in the management of severe respiratory symptoms in coronavirus-infected patients in the past. However, there remains no definitive evidence in the literature for or against the utilization of systemic glucocorticoids in seriously ill patients with coronavirus-related severe respiratory disease, or indeed in other types of severe respiratory disease. In this study, we hope to discover evidence either supporting or opposing the systemic therapeutic administration of glucocorticoids in severe coronavirus disease 2019 (COVID-19) patients.
Trial registration:ClinicalTrials.gov, ChiCTR2000029386, http://www.chictr.org.cn/showproj.aspx?proj=48777.
