EUCTR2016-001876-31-GB进行中(未招募)1 期
Feasibility of the safe withdrawal of inhaled corticosteroids in patients with mild to moderate COPD prescribed outside guidelines (SWAP) - SWAP
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 入组人数
- 106
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •1) known diagnosis of mild or moderate COPD (forced expiratory volume in first second (FEV1) =50% predicted and FEV1/forced vital capacity (FVC) <0.7) obtained from spirometry within the past 12 months and confirmed at interview
- •2) prescribed and have used high-dose ICS (alone or in combination with a long-acting bronchodilator) at a dose of fluticasone propionate =250mcg/day, fluticasone furoate =92mcg/day, budesonide >400mcg/day or beclomethasone dipropionate >400mcg/day on most days for at least 3 months
- •3) aged =45 years
- •4) <2 exacerbations in the previous year and no admissions to hospital with an exacerbation since the diagnosis of COPD was made
- •5) BMI of less than 35.
- •Are the trial subjects under 18? no
- •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 106
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 106
排除标准
- •1) a history (stated in the patient record) of asthma, lung cancer or breathlessness secondary to cardiac disease
- •2) current severe mental illness (severe depression or psychosis)
- •3) current alcohol dependence (patient report or entry in medical record as alcohol dependence or alcohol induced disease)
- •4) Patients diagnosed with dementia
- •5) Patients who use continuous oral corticosteroids
- •6) Patients who are unwilling or unable to follow the study protocol
- •7) Patients who are participating in another clinical trial
- •8) Pregnant females or females of childbearing age not using effective contraception
研究者
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