Abstract

BackgroundCough variant asthma (CVA) is one of the leading causes of chronic coughing. The main treatment is currently anti-inflammatory medication. However, the coughing may return or be aggravated and lung function may deteriorate once the anti-inflammatory treatment is stopped. The effect of Chinese herbal medicine (CHM) on chronic coughing is remarkable, but high-quality evidence supporting its effectiveness is still lacking. This trial aims to evaluate the safety and efficacy, especially the long-term efficacy, of CHM plus anti-inflammatory medications for the treatment of CVA.Methods/designA randomized placebo-controlled double-blind trial will be conducted. It will consist of a 3-month intervention followed by a 6-month follow-up period.The target sample size is 60 patients with CVA who are between 18 and 70 years old. The eligible subjects will be allocated randomly into the experimental or control group in a ratio of 1:1. Patients in the experimental group will take CHM granules (4.9 g twice daily), while patients in the control group will be given a matched placebo. An administration of salmeterol/fluticasone propionate combination for 12 weeks will be the basic therapy for the two groups. The primary outcome is the cough visual analog scales (CVAS). The secondary outcomes include quality of life, rate of symptom relapse, lung function, and blood tests. A safety assessment will also be performed during the trial.DiscussionThe evidence gathered by the trial will be a valuable addition to informing treatment options for patients with CVA.Trial registrationhttp://www.chictr.org.cn, ID: ChiCTR-IOR-16009148. Registered on 3 September 2016.

Highlights

  • Cough variant asthma (CVA) is one of the leading causes of chronic coughing

  • The evidence gathered by the trial will be a valuable addition to informing treatment options for patients with CVA

  • It is reported that Chinese herbal medicine (CHM) plus ICS/LABA is better at reducing cough symptom scores, improving lung function, and improving quality of life compared with ICS/LABA alone [10,11,12]

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Summary

Discussion

This is the first clinical study to investigate the long-term efficacy of CHM plus ICS/LABA for CVA. If the CHM granule plus ICS/LABA treatment is found to be safe and effective in the long term for CVA patients, it will be a great help in resolving this problem. The results of this trial will provide highquality evidence of the efficacy of CHM in the treatment of CVA.

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