Comparing Morning and Evening Dosing of Inhaled Long-Acting Muscarinic Antagonists for the Prevention of Hospitalization Requiring AECOPD or Death from All Causes - the LAMA by Night Study Utilizing a Comprehensive Nationwide Digital Platform for Recruitment Into a Pragmatic Randomized Controlled Trial Integrated with National Registries to Follow Outcomes
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 10,011
- 试验地点
- 1
- 主要终点
- All-cause mortality
研究概览
简要总结
To examine, among once-daily LAMA using COPD patients, whether evening administration of LAMA is superior with respect to the incidence of hospitalization requiring AECOPD or death from all causes than the more conventional morning administration.
详细描述
One of the most feared complications associated with chronic obstructive pulmonary disease (COPD) is acute exacerbation (AECOPD). On average, each COPD patient experiences 0.5 to 3.5 acute exacerbations per year, which is an important reason for the hospitalization, disease progression and mortality as well as decline in health status and lung function(1,2).
Treatment with a long-acting muscarinic antagonist (LAMA) reduces dyspnoea and the risk of exacerbations in patients with COPD by binding to muscarinic receptors in bronchial smooth musculature and thus inhibiting cholinergic bronchial constriction. LAMAs are given as inhalation therapy once daily (most often) or twice daily(3).
Most COPD-patients experience their worst symptoms and experience exacerbations in early morning hours, before getting out of bed(4). This might be explained by the physiological diurnal changes in the activity of the parasympathetic homeostasis system since this is most active at night to improve digestion and other secretions(5).
Correspondingly, the activity of the sympathetic system is physiologically suppressed at night, and stimulation of β-2 receptors is thus also low (and opposite for M-3 receptors). Taken together, the balance of sympathetic-parasympathetic tone is shifted significantly towards the latter. Most available LAMA treatments are dosed once daily in the morning.
Thus, for a COPD patient, being at a trough level of LAMA (which antagonizes the para-sympathetic system) at late night/early morning, may carry a hazard for the patient.
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 (Investigator, Outcomes Assessor)
盲法说明
Investigators will be blinded for the treatment allocation, but the trial participants will not be blinded. However, since all endpoints are assessed using prespecified registry-based definitions, bias should be negligible.
入排标准
- 年龄范围
- 30 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age more than or equal to 30 years
- •Current treatment with LAMA once daily (as recorded in the Danish National Prescription Registry and confirmed by the participant via questionnaire)
- •Self-reported COPD
排除标准
- •Patients who decline to participate.
研究组 & 干预措施
Bedtime administration of LAMA
Participants randomized to this group (with or without the combination of inhaled corticosteroids (ICS) and/or long-acting beta2-agonists (LABA)) will be instructed to take their LAMA-containing inhalation between 8pm. and 2am.
干预措施: Long acting muscarinic antagonists (LAMAs) in the evening (Drug)
结局指标
主要结局
All-cause mortality
时间窗: 12 months from randomization
COPD-related hospitalization-requiring (severe) exacerbations
时间窗: 12 months from randomization
次要结局
- Moderate, non-hospitalization-requiring COPD exacerbations(12 months from randomization)
- Number of admissions for all causes(12 months from randomization)
- Number of admissions requiring non-invasive ventilation (NIV) treatment(12 months from randomization)
- Use of short-acting β2-agonists (SABA); pick-up rate(12 months from randomization)
- Number of admissions in the intensive care unit (ICU) for all causes(12 months from randomization)
- Mortality (all-cause)(12 months from randomization)
- Change in COPD assesment test (CAT) score(12 months from randomization)
- Change in medical research council (MRC) score(12 months from randomization)
