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临床试验/ISRCTN23547970
ISRCTN23547970已完成未知

A feasibility randomised controlled trial investigating the clinical and cost effectiveness of a complex intervention to improve the management of children presenting to primary care with acute respiratory tract infection

niversity of Bristol (UK)0 个研究点目标入组 500 人开始时间: 2014年6月27日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
500

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

  • Clinicians:
  • GPs and prescribing nurses are eligible to recruit children to the study
  • GP practices will be included if they have at least Internet Explorer version 8 on their IT systems
  • Children can be included into the study if they meet the following criteria:
  • 1. Children aged =3 months and <12 years
  • 2. Presenting with an acute RTI with cough for =28 days as a main symptom (including exacerbation of asthma)
  • 3. Presenting with illnesses such as RTI and epilepsy or diabetes, including infective exacerbation of asthma (non-infective exacerbation of asthma is an exclusion criterion)
  • Target Gender: Male & Female; Upper Age Limit 11 years ; Lower Age Limit 3 months

排除标准

  • Children will not be eligible for the study if:
  • 1. They are aged < 3 months or = 12 years
  • 2. The parent/carer/children are unable or unwilling to assist with study
  • 3. The child has already been successfully recruited to the CHICO study
  • 4. They present with acute non-infective exacerbations of asthma
  • 5. They present with RTI without cough or symptoms >28 days
  • 6. They are at greater risk of serious infection; they have chronic diseases/multi-morbidities that increase the risk of RTI complications

研究者

发起方
niversity of Bristol (UK)

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