跳至主要内容
临床试验/ISRCTN10204126
ISRCTN10204126进行中(未招募)Unknown

Perpetual Observational Study of Acute Respiratory Infections in primary care settings (PC) across Europe (POS-ARI-PC)

European Clinical Research Alliance for Infectious Diseases (Ecraid)0 个研究点目标入组 8,400 人开始时间: 2023年7月20日最近更新:
适应症

试验速览

阶段
Unknown
状态
进行中(未招募)
发起方
入组人数
8,400

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • Eligible patients will be of any age consulting (telephone, video, face to face) with a participating primary health care facility with:
  • 1. Symptoms suggestive of an acute lower respiratory infection with cough as the predominant symptom, with illness duration less than 28 days,
  • 2. Symptoms suggestive of an acute upper respiratory infection with a sore throat and/or coryza as the predominant symptom, with illness duration of less than 14 days
  • 3. Other symptoms suggestive of COVID-19, Influenza, RSV
  • 4. Participant or legal guardian(s) willing and able to provide informed consent and comply with study procedures
  • (added 28/02/2024)
  • POS-ARI-PC-001 Study
  • 1. Eligible patients will be 60 years of age and over consulting (telephone, video, or face-to-face in the practice, or home visit ) with a participating primary health care facility with:
  • 1.1. Symptoms suggestive of an acute lower RTI with new or increased cough as the predominant symptom, with illness duration <=7 days; AND/OR
  • 1.2. Symptoms suggestive of an acute upper RTI with sore throat and/or coryza as the predominant symptoms, with illness duration <=7 days; AND
  • 1.3. Willing and able to provide informed consent and have a swab taken

排除标准

  • Patients will not be eligible if:
  • 1. According to the judgement of the recruiting clinician, they will not be able to comply with study procedures, for example, because they do not understand the language in which the study is being conducted locally (and have no one to help and translate for them); have a serious psychiatric disorder; or are terminally ill
  • 2. Symptoms of presumed non-infective origin
  • 3. Participant requires admission to the hospital on the day of inclusion. Additional in/exclusion criteria might apply to embedded studies and will be described in the SSA or ISA
  • (added 28/02/2024)
  • POS-ARI-PC-001 Study
  • As per the POS-ARI-PC CORE Protocol, with one exception: patients needing hospitalisation can be recruited into the study if timing allows. Patients can provide a swab and decide not to participate in the follow-up procedures.

研究者

发起方
European Clinical Research Alliance for Infectious Diseases (Ecraid)

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