跳至主要内容
临床试验/NCT05855395
NCT05855395招募中不适用

A Bidimensional Early Intervention Strategy of Standard of Care Combined With Host Immunomodulation in Elderly Patients With Mild or Moderate COVID-19: A Multicentre, Randomized, Controlled, Adaptive Platform Study

Huashan Hospital15 个研究点 分布在 1 个国家目标入组 5,815 人开始时间: 2023年5月26日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
招募中
入组人数
5,815
试验地点
15
主要终点
Proportion of patients who progress to severe or critical COVID-19 within 28 days

研究概览

简要总结

This study is aimed to explore the dual-dimensional early intervention strategy of standard of care combined with host immunomodulation in elderly patients with mild and moderate COVID-19.

详细描述

In this multicentre, randomized, controlled, and adaptive platform trial exploring the efficacy and safety of short-term and low-dose glucocorticoid combined with standard of care in mild or moderate elderly patients (with or without other high-risk factors) who are over 65 years.We are looking for the best treatment strategy to prevent mild or moderate COVID-19 from developing into severe/critical COVID-19, so as to reduce the risk of disease progression and death in the elderly patients and benefit more patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age ≥ 65;
  • •Male or female;
  • •Positive test for coronavirus antigen or nucleic acid;
  • •Within 7 days of onset (fever and/or cough) ;
  • •mild and moderate;Mild: respiratory tract infection is the main manifestation, such as dry throat, sore throat, cough, fever;Moderate: continuous high fever>3 days or (and) cough, shortness of breath, etc., but respiratory rate (RR)<30 times/minute, oxygen saturation>93% when breathing air at rest. Imaging findings of characteristic pneumonia caused by COVID-19 infection;
  • •The patient is willing to participate in the trial treatment and follow-up, and sign the informed consent form (if the patient lacks the ability to give informed consent due to his serious medical condition, such as acute respiratory failure or the need for respiratory support, he can obtain the consent of the patient's legal representative);
  • •No systemic glucocorticoids treatment in the past 7 days;

排除标准

  • •Serious and uncontrolled comorbidities;
  • •Expected lifetime is less than 1 month;
  • •Severe/critical;
  • •Other situations that are evaluated by researchers as not suitable for participating the study.
  • •Criteria for discontinuation
  • •The subject could not benefit after treatment (discontinued patients could be analyzed according to the PP analysis set);
  • •Withdrawal criteria (if any of the following items are required)
  • •The subject asked to withdraw from the study;
  • •The subject needs to withdraw from the study after clinical observation after discontinuing treatment;
  • •The subject died or lost to follow-up.

研究组 & 干预措施

Group A

Experimental

Experimental group with standard of care combined with glucocorticoid(dexamethasone: 3mg qd x 5 days; or prednisone: 20mg qd x 5 days; or methylprednisolone: 16mg qd x 5 days)

干预措施: Glucocorticoid (Drug)

结局指标

主要结局

Proportion of patients who progress to severe or critical COVID-19 within 28 days

时间窗: In 28 days

Definition of severe COVID-19 1. At rest, oxygen saturation ≤ 93% when inhaling air; 2. Progression due to COVID-19 (defined as \>50% of significant progression of lesions within 24\~48 hours on lung imaging; or respiratory failure requiring mechanical ventilation; or emergency department visits or hospitalizations with shock) and/or complications (comitant other organ failure requiring intensive care unit monitoring).

次要结局

  • Days of respiratory symptoms(In 28 days)
  • Proportion of patients who progress to severe or critical COVID-19 within 28 days(In 28 days)
  • Length of hospital stay for any reason(In 28 days)
  • Duration of antigen or nucleic acid negative conversion(In 28 days)
  • Day 14 antigen or nucleic acid conversion rate(Day 14)
  • All-cause mortality(In 28 days)
  • Duration of outpatient hospitalization/emergency department visits due to COVID-19 progression(from the date of enrollment)(In 28 days)
  • Proportion of emergency department visits or hospitalizations due to COVID-19 progression(In 28 days)
  • Time for initial symptom relief,Duration of symptom relief(In 14 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wen-hong Zhang

Director of Division of Infectious Diseases Affiliation: Huashan Hospital

Huashan Hospital

研究点 (15)

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