Situations That do Not Require Antibiotics for Acute Exacerbations of Mild-to-moderate Chronic Obstructive Pulmonary Disease
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 318
- 试验地点
- 13
- 主要终点
- Number of Patients Who Were Cured
研究概览
简要总结
The purpose of this study is to determine the effectiveness of antibiotic therapy for patients with acute exacerbations of mild-to-moderate chronic obstructive pulmonary disease.
详细描述
Antibiotics are usually prescribed for acute exacerbations of chronic obstructive pulmonary disease (COPD) even though their benefit in mild-to-moderate COPD is not demonstrated. The aim of this study is to assess the effectiveness of antibiotic therapy for exacerbations of COPD, what clinical variables are associated with an improved clinical response with antibiotic therapy with respect to placebo and to identify which patients might recover from an acute exacerbation without antibiotic therapy. Methodology: prospective, randomised, double blind, placebo-controlled clinical trial, in which exacerbations (at least one criterion present: increase of dyspnoea, increase of sputum production and/or increase of purulence) of patients older than 40 yr., smokers or ex-smokers of more than 10 pack-years, with COPD and FEV1 greater than 50%, diagnosed by spirometry and a predicted ratio FEV1/FVC<0.7%. Exclusion criteria: severe COPD (FEV1<50%), active neoplasm, tracheotomy, pneumonia, hospitalization criteria, patients previously being on antibiotics, immunodepressed, history of hypersensitivity to beta-lactams or intolerance to clavulanate, enrollment in other clinical trials, patients who refuse to take part in this study, and patients who have not had a spirometry test for the past two years. Sample size: 677 patients. Interventions: first visit: the patient will be given details of the clinical trial and will be asked to sign informed consent; other data: sputum color, chest X-ray ordered to rule out pneumonia, C-reactive protein levels, and peak flow measurement. The patient will be randomised to receive amoxicillin plus clavulanate or placebo and will be scheduled to return for a 2nd follow-up visit after 3 or 4 days to assess the clinical response and peak flow measurements and to rule out any worsening of the condition. Third visit: scheduled after 9-11 days to assess the clinical response, drug-compliance and peak flow measurement. Fourth visit after 15-20 days for clinical assessment and to observe whether any relapses have occurred. Date of the following exacerbation will be recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 40 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Acute exacerbations (at least one criterion present: increase of dyspnoea, increase of sputum production and/or increase of purulence) of
- •patients older than 40 years old,
- •smokers or ex-smokers of more than 10 pack-years,
- •with COPD and FEV1 greater than 50%, diagnosed by spirometry and a predicted ratio FEV1/FVC<0.7%.
排除标准
- •Severe COPD (FEV1<50%)
- •Pneumonia
- •Active neoplasm
- •Tracheotomy
- •Criteria for hospitalisation
- •Patients previously being on antibiotics
- •Immunodepressed patients
- •History of hypersensitivity to beta-lactams or intolerance to clavulanate
- •Enrollment in other clinical trials
- •Patients who refuse to take part in this study
- •Patients who have not had a spirometry test for the past two years
研究组 & 干预措施
Placebo
Placebo pills t.i.d. for 8 days
干预措施: Placebo (Drug)
Amoxycillin and clavulanic acid
Amoxycillin and clavulanate t.i.d. for 8 days
干预措施: Amoxicillin and clavulanic acid (Drug)
结局指标
主要结局
Number of Patients Who Were Cured
时间窗: Day 9-11
Cure defined as the disappearance of the acute signs and symptoms related to the infection, with complete return to the previous situation of stability
次要结局
- Number of Days Till the Next Exacerbation(One year)
研究者
Carl Llor
Doctor
Catalan Society of Family Medicine
