跳至主要内容
临床试验/ISRCTN55471843
ISRCTN55471843进行中(未招募)未知

European Clinical Research Alliance on Infectious Diseases – PRIMary care adaptive platform trial for pandemics and Epidemics

niversity Medical Center Utrecht0 个研究点目标入组 1,700 人开始时间: 2022年11月21日最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
入组人数
1,700

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • In order to be eligible to participate in ECRAID-Prime, a participant must (at least) meet all the following criteria (there can be additional intervention-specific inclusion criteria):
  • 1. Participant is =18 years of age on the day of inclusion; if people aged <18 years are suitable for inclusion in the evaluation of an investigational product, then this will be described and justified in the relevant, approved intervention-specific appendix
  • 2. Presence of at least two symptoms suggestive of COVID-19 or COVID-like-illness, one respiratory (cough, sore throat, running or congested nose or sinuses, shortness of breath) and one systemic (fever, feeling feverish, sweats/chills or shivering, low energy or tiredness, headache, muscle, joint or body aches, loss of taste and/or smell)
  • 3. Judged by recruiting a medically qualified clinician or research nurse that the illness is due to COVID-19 or COVID-like illness
  • 4. Onset of symptoms less than 7 days (in case earlier treatment is required for a specific investigational product, this will be specified in the intervention-specific appendix)
  • 5. Willing and able to give informed consent for participation in the study
  • 6. Willing and able to comply with all trial procedures
  • 7. Any additional eligibility criteria relevant to women of child-bearing potential including current pregnancy or breastfeeding will be specified in the intervention-specific appendix

排除标准

  • A potential participant who meets any of the following criteria will be excluded from participation in ECRAID-Prime (there can be additional intervention-specific exclusion criteria).
  • 1. Requiring admission to the hospital on the day of screening, or inclusion
  • 2. Known allergies or hypersensitivities to any of the components used in the formulation of the investigational product, or the control product
  • 3. Any disease, condition, or disorder that precludes participation in the trial, in the opinion of the person checking eligibility and taking consent
  • 4. Any planned major surgery in the next 28 days
  • 5. Currently participating in a trial of an investigational product

研究者

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