跳至主要内容
临床试验/NCT04591613
NCT04591613招募中不适用

Late Clinical Events Associated With COVID-19 Infection: Multicenter Cohort

Tourcoing Hospital12 个研究点 分布在 2 个国家目标入组 1,000 人开始时间: 2020年12月31日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
1,000
试验地点
12
主要终点
Clinical description of asthenia

研究概览

简要总结

Several publications document the occurrence of symptoms that persist or occur late.

The identification of the observed clinical manifestations and their clinical and paraclinical description are essential to better understand the natural evolution of COVID-19, to clarify the pathophysiological mechanism of these possible late manifestations, and to identify potential management options for patients.

Since this type of event is infrequent, a large-scale national multicenter cohort study focusing on symptomatic patients is needed.

详细描述

Several publications document the occurrence of symptoms that persist or occur late, more than 3 weeks after the first clinical manifestations of an SARS-COV2 infection. These manifestations may be related to thromboembolic or inflammatory complications, superinfections, or other mechanisms not yet well understood, including potentially related to the persistence of SARS-COV2. The identification of the observed clinical manifestations and their clinical and paraclinical description are essential to better understand the natural evolution of COVID-19, to clarify the pathophysiological mechanism of these possible late manifestations, and to identify potential management options for patients.

Since this type of event is infrequent, a large-scale national multicenter cohort study focusing on symptomatic patients is needed. In parallel, the prevalence of the main symptoms observed more than 3 weeks after the onset of a COVID-19 will be estimated through partnerships with existing cohort studies in the general population or in the population followed for COVID-19, still symptomatic or not at 3 weeks of infection.

Longitudinal implementation of bio-libraries will allow this cohort to also constitute a bridge between clinicians and researchers.

研究设计

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

入排标准

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

入选标准

  • History of symptomatic CoV-2-SARS infection as defined by :
  • o Positive RT-PCR SARS-CoV-2 RT-PCR result OR positive SARS-CoV-2 serology
  • o Associated with at least one event : x Anosmia occurring after February 2020 x OR COVID 19 evocative scanner x OR ≥ 2 contemporary symptoms of the virological sample from: asthenia, cough, dyspnea, fever, myalgia, dysgeusia, diarrhea AND not present prior to diagnosis
  • AND persistence of at least one symptom present in the first 3 weeks of a COVID-19, more than 8 weeks away from the first symptoms of COVID-
  • OR late onset of at least one new symptom a minimum of 3 weeks and a maximum of 6 months after the first symptoms of a CoV-2 SARS infection.
  • First symptoms less than 6 months old on the day of inclusion
  • To benefit from a State Health Insurance or Medical Aid plan
  • Have signed an informed consent for inclusion.

排除标准

  • Minor patient
  • Patient under protection of justice
  • Patient who required intensive care management :
  • more than 5 days
  • OR requiring orotracheal intubation
  • OR having required high flow ventilation (optiflow)

结局指标

主要结局

Clinical description of asthenia

时间窗: At the end od the study, an average of 22 months

Describe the frequence of asthenia between its onset and its disappearance. Assessment at baseline, then 4, 6 and 12 months.

Clinical description of dyspnea

时间窗: At the end od the study, an average of 22 months

Frequence of dyspnea between its onset and its disappearance. Assessment at baseline, then 4, 6 and 12 months. Assessment at baseline, then 4, 6 and 12 months.

Clinical description of anosmia

时间窗: At the end od the study, an average of 22 months

Frequence of anosmia disorders between its onset and its disappearance. Assessment at baseline, then 4, 6 and 12 months. Assessment at baseline, then 4, 6 and 12 months.

Clinical description of neurological disorders

时间窗: At the end od the study, an average of 22 months

Frequence of neurological disorders between its onset and its disappearance. Assessment at baseline, then 4, 6 and 12 months. Assessment at baseline, then 4, 6 and 12 months.

Clinical description of thoracic disorders

时间窗: At the end od the study, an average of 22 months

Frequence of thoracic disorders between its onset and its disappearance. Assessment at baseline, then 4, 6 and 12 months. Assessment at baseline, then 4, 6 and 12 months.

次要结局

未报告次要终点

研究者

发起方
Tourcoing Hospital
申办方类型
Other
责任方
Sponsor

研究点 (12)

Loading locations...

相似试验

Late Clinical Events Associated With COVID-19... | 临床试验