The purpose of this study is to investigate the efficacy and safety of procaterol hydrochloride with inhaled glucocorticoid in treatment patients with cough variant asthma (CVA).
This is a 8-week, double-blind, randomized, placebo-controlled study, the patients with CVA will be randomized to experimental or placebo control group. During the screening period, eligible patients will be evaluated by cough symptom score and LCQ life quality score. After 4 and 8 weeks treatment, patients will be evaluated by cough symptom score and LCQ life quality score respectively. Adverse events will also be captured at every visit.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
160
25µg BID for 8 weeks
25µg BID for 8 weeks
Xin Zhou
Shanghai, Shanghai Municipality, China
Patient cough symptom score
Time frame: 8 weeks
Therapy duration
Time frame: 8 weeks
Rates of adverse events
Time frame: 8 weeks
LCQ Life Quality Score
Time frame: 8 weeks
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