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临床试验/JPRN-UMIN000031039
JPRN-UMIN000031039已完成未知

Comparison of clinical efficacy between fluticasone propionate/ formoterol (FFC) and fluticasone furoate/ vilanterol (VFC) in patients with asthma - Comparison of clinical efficacy between FFC and VFC

Ikeda Clinic0 个研究点目标入组 24 人开始时间: 2018年1月29日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
24

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Patients with evident ACO or COPD comorbidities 2. Patients with antibiotic-resistant infections, deep mycosis, or tuberculosis disease 3. Patients who have been afflicted with a respiratory infection (viral infection) within 8 weeks prior to enrollment 4. Patients with a smoking history of at least 10 pack years 5. Patients who have experienced side effects from the use of ICS, LABA or the combined medications 6. Patients who have used systemic steroids within 4 weeks prior to enrollment 7. Patients with significant heart, liver, kidney disease or other clinically significant comorbidities 8. Patients who are pregnant, breastfeeding, or plan to become pregnant during the study period 9. Other patients who are judged unsuitable for inclusion by the investigators in the study

研究者

发起方
Ikeda Clinic

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