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临床试验/NCT04377477
NCT04377477已完成不适用

Pilot Study on the Feasibility of Low Dose Radiotherapy for SARS-Cov-2 Pneumonitis (COVID-19 Low Dose Radiotherapy - COLOR 19)

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia2 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2020年5月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
3
试验地点
2
主要终点
Number of Intensive Care Unit admissions

研究概览

简要总结

Low-dose radiotherapy treatment delivered to both lungs in patients with immune-related pneumonia following COVID-19 infection is backed up by biological and clinical bases that justify its use as a possible therapeutic option in these patients. This is a preliminary exploratory study (non-pharmacological interventional) to evaluate the feasibility and tolerability of low-dose radiotherapy treatment of SARS-Cov-2 immune-mediated pneumonia, for the subsequent implementation of a phase II study.This is a preliminary, monocentric, single-arm, interventional, non-pharmacological exploratory study. All enrolled patients will be treated with low-dose radiotherapy. Participants will undergo irradiation of the lungs, administered in a single fraction at the average prescription dose of 0.7 Gy (further details in the dedicated section).

详细描述

BACKGROUND

Since the first case of Severe Acute Respiratory Syndrome - Coronavirus - 2 (SARS-CoV-2) infection and its subsequent clinical manifestation (COronaVIrus Disease 19, COVID-19) in the city of Wuhan (Hubei, China) in December 2019, contagion abruptly spread to different regions of China and, subsequently, to all continents. To date, 1 521 252 cases have been confirmed worldwide. With the first case ascertained in Lombardy at the end of February 2020, Italy soon became the first European country to face the exponential growth in the number of infected people (to date -May 3, 2020-210,717 total cases, currently positive 100,179).The disease turned into an actual health emergency due to the rapid spread and the need of hospitalization and respiratory function support in Intensive Care Unit (ICU) for a significant fraction of the patients. However, the clinical presentation of COVID-19 is non-specific and extremely heterogeneous. Many patients are asymptomatic or exhibit mild symptoms, which include cough, fever, general malaise with myalgias, anosmia and ageusia. The most common changes in blood tests include lymphopenia, thrombocytopenia and increased C-reactive protein and ferritin.

As emerged by clinical data, the viral infection could be divided into three different phases: stage I, asymptomatic incubation period with little or undetectable viral load; stage II, mild symptomatic period with considerable and detectable viral load; stage III, severe symptomatic period with high viral load.

The definitive diagnosis requires a positive molecular test with Real Time PCR (RT-PCR) method for SARS-CoV-2 on nasopharyngeal swab. However, this technique suffers from sub-optimal sensitivity, which may require repetition on bronchoalveolar lavage. The execution of chest CT is therefore essential, as it is characterized by high sensitivity and can detect highly suggestive findings even in patients with negative RT-PCR.

Although the majority of infections resolve spontaneously without the need for specific therapy, up to 20% of patients can develop severe clinical pictures with pneumonia characterized by dyspnea, tachypnea and hypoxemia that requires treatment in a hospital setting. Pulmonary involvement is typically bilateral, peripheral and basal in most cases, presenting on CT scan with multifocal ground glass opacities and interstitial infiltrations; complete resolution usually takes several weeks. Despite active treatment, about 5-10% of cases can precipitate, often suddenly, into critical conditions including respiratory failure, ARDS and multi-organ dysfunction that require ICU admission and are burdened with high mortality.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • 未提供

排除标准

  • Age <50 years
  • Brescia Covid Respiratory Severity Scale (BCRSS) score greater than 3
  • Patients undergoing invasive mechanical ventilation
  • Patients with active autoimmune systemic diseases
  • Patients with active infections that are not responsive to current treatment
  • Patients with a positive pregnancy test
  • Impossibility to maintain the set-up necessary for radiotherapy treatment
  • Other concomitant treatments for COVID-19 do not represent an exclusion criterion, however they must be reported (specifying the starting date and dosage)

结局指标

主要结局

Number of Intensive Care Unit admissions

时间窗: Six months

Evaluation of the feasibility of low-dose radiotherapy treatment of SARS-Cov2 pneumonia; the number of intensive care unit admissions will be recorded

Lenght of hospital stay (days)

时间窗: Six months

Evaluation of the feasibility of low-dose radiotherapy treatment of SARS-Cov2 pneumonia, for the purpose of the subsequent implementation of a phase II study; lenght of hospital stay will be recorded

次要结局

  • Variation of the Brescia COVID-19 Respiratory Severity Scale after treatment(3, 6 and 10 days)
  • Occurence of CTCAE 5.0 adverse events(10 days and 6 months)
  • Variation of the chest X-ray radiological findings according to Brixia scoring system(3 and 6 days)

研究者

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

Stefano Maria Magrini

Prof

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

研究点 (2)

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