跳至主要内容
临床试验/JPRN-UMIN000049879
JPRN-UMIN000049879招募中4 期

Efficacy, equivalence and operability of switching to a combination of budesonide, glycopyrronium, and formoterol in patients with COPD and ACO - Efficacy, equivalence and operability of switching to a combination of budesonide, glycopyrronium, and formoterol in patients with COPD and ACO

Kindai University Nara Hospital0 个研究点目标入组 70 人开始时间: 2022年12月23日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
70

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
40years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Under 40 years old 2) Patients who have difficulty inhaling by theirself 3) Patients for whom the physician determines that pulmonary function testing is impossible or inaccurate for any reason (e.g., hearing loss, pregnancy, etc.) 4) Patients whose QoL or lung function may be affected during the study period, as determined by the physician: e.g., patients with end-stage cancer, severe heart failure, liver cirrhosis, respiratory failure, etc. 5) Patients who cannot use ICS or LABA or LAMA

研究者

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