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 RTI

niversity of Southampton0 个研究点目标入组 889 人2008年2月22日

概览

阶段: 1 期
干预措施: 未指定
疾病 / 适应症: Inclusion 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.
发起方: niversity of Southampton
入组人数: 889
状态: 进行中（未招募）
最后更新: 5年前

暂无简介。

注册库

who.int

开始日期

2008年2月22日

结束日期

2013年12月3日

最后更新

5年前

研究类型

Interventional clinical trial of medicinal product

性别

All

发起方

niversity of Southampton

•Inclusion criteria
•Patients aged 3 to 65 presenting to a 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).
•Are the trial subjects under 18? yes
•Number of subjects for this age range:
•F.1\.2 Adults (18\-64 years) yes
•F.1\.2\.1 Number of subjects for this age range
•F.1\.3 Elderly (\>\=65 years) no
•F.1\.3\.1 Number of subjects for this age range

•Exclusion criteria
•(i) active or previous peptic ulceration
•(ii) hypersensitivity to aspirin ibuprofen or paracetamol
•(iii) inability to measure temperature or complete outcome measures (e.g. parents visually impaired, psychosis, severely depressed)
•(iv) patients requiring hospital admission (e.g. suspected meningitis, severe pneumonia, epiglottitis, Kawasaki's disease etc),
•(v) patients with known immune deficiency (where the course of illness and symptomatic response might be modified)
•(vi) pregnancy or breastfeeding