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临床试验/EUCTR2016-001876-31-GB
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

King's College London0 个研究点目标入组 106 人开始时间: 2016年8月5日最近更新:
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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