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临床试验/JPRN-UMIN000016856
JPRN-UMIN000016856已完成未知

Evaluation of the clinical efficacy of flutiform®(fluticasone propionate /formoterol fumarate) on severe persistent bronchial asthma - Evaluation of the clinical efficacy of flutiform®(fluticasone propionate /formoterol fumarate) on severe persistent bronchial asthma

Dokkyo Medical University Hospital0 个研究点目标入组 30 人开始时间: 2015年3月20日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
30

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 COPD (2)Patients who take SABA other than treatment of exacerbations (3)Patients who had a history of adverse reaction to ICS or LABA (4)Patients who took flutiform ® within four weeks (5)Patients with severe cardiac, hepatic, renal, pulmonary, or hematologic disease (6)Current malignancy (7)Smoking within past 1 year (8)Those who are pregnant, under-lactation, or desire pregnancy (9)Unsuitability as determined by the investigator

研究者

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