ISRCTN38551726已完成不适用
A pragmatic randomised trial of ibuprofen, paracetamol, steam and delayed prescribing for patients with respiratory tract infections in Primary Care
niversity of Southampton (UK)0 个研究点目标入组 504 人开始时间: 2009年3月12日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 504
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
- •1. Aged 3 years and over, either sex
- •2. Presenting to a General Practitioner (GP) or nurse with an RTI diagnosed by the health professional (acute cold, influenza, sore throat, otitis media, sinusitis, croup, or lower respiratory tract infection)
排除标准
- •1. Active or previous peptic ulceration
- •2. Hypersensitivity to aspirin ibuprofen or paracetamol
- •3. Inability to measure temperature or complete outcome measures (e.g. parents visually impaired, psychosis, severely depressed)
- •4. Patients requiring hospital admission (e.g. suspected meningitis, severe pneumonia, epiglottitis, Kawasaki's disease, etc.)
- •5. Patients with known immune deficiency (where the course of illness and symptomatic response might be modified)
- •6. Pregnancy or breastfeeding
研究者
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A Pragmatic Randomised Trial of Ibuprofen, Paracetamol, Steam and Delayed Prescribing for Patients with Respiratory Tract Infections in Primary Care - Trial of ibuprofen, paracetamol, steam and delayed prescribing for RTIInclusion criteriaPatients aged 3 to 65 presenting to a GP or nurse with an RTI (acute cold, influenza, sore throat, otitis media, sinusitis, croup, or lower respiratory tract infection). Exclusion criteriaActive or previous peptic ulceration, hypersensitivity to aspirin ibuprofen or paracetamol, inability to measure temperature or complete outcome measures, patients requiring hospital admission, patients with known immune deficiency, pregnancy or breastfeeding.MedDRA version: 8.1Level: HLGTClassification code 10024970Term: Respiratory tract infectionsEUCTR2006-005740-83-GBniversity of Southampton889
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