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白三烯受体拮抗剂与喘证宝合汤联合治疗哮喘患者的效果:一项随机、安慰剂对照、平行、多中心试验方案

Effect of add-on therapy with leukotriene receptor antagonists and Chungsangboha-tang in patients with asthma: a protocol for a randomized, placebo-controlled, parallel, multicenter trial.

作者信息

Kang Sung-Woo, Nam Hae-Seong, Park Yang-Chun, Choi Jun-Yong, Kim Ki-Tae, Ha Seo-Jung, Kim Kwan-Il, Jung Hee-Jae, Lee Beom-Joon

机构信息

Department of Clinical Korean Medicine, College of Korean Medicine, Graduate School, Kyung Hee University, Seoul, 02447, Republic of Korea.

Division of Pulmonology, Department of Internal Medicine, Inha University Hospital, Inha University School of Medicine, Incheon, 22332, Republic of Korea.

出版信息

BMC Complement Med Ther. 2025 Feb 14;25(1):54. doi: 10.1186/s12906-025-04799-w.

Abstract

BACKGROUND

Asthma is a chronic disease characterized by airway inflammation and obstruction. Treatment aims to control symptoms with minimal medication, using disease-controlling and symptom-relieving drugs. Inhaled steroids and beta2 agonists are common treatments; however, their long-term use can cause side effects. Leukotriene receptor antagonists (LTRAs) are used in combination with inhaled steroids to manage asthma because of their anti-inflammatory and bronchodilatory effects. Combining LTRAs with Chungsangboha-tang (CSBHT), a Korean medicine, may enhance their efficacy. This study aimed to evaluate the potential of CSBHT as an adjunctive therapy for asthma management in a randomized, placebo-controlled, double-blind, multicenter clinical trial.

METHODS

This randomized, placebo-controlled, double-blind, parallel-group, multicenter study aims to evaluate the efficacy and safety of CSBHT as an additional treatment for patients with asthma, particularly for those with LTRAs. Overall, 198 participants will be randomly divided into intervention and control groups, with the former receiving CSBHT thrice daily and the latter receiving a placebo. Follow-ups at weeks 0, 4, and 8 will include outcome measurements, medication dispensation, and adverse reaction monitoring. The primary outcome is the mean change in forced expiratory volume in one-second scores, with secondary outcomes including changes in peak expiratory flow, forced vital capacity, forced expiratory flow 25-75%, fractional exhaled nitric oxide, Asthma Control Test, Asthma Quality of Life Questionnaire, serum IgE, eosinophil count, C-reactive protein, rescue medication usage, and a descriptive analysis of the questionnaire on asthma symptoms in Korean medicine. Safety assessments will be conducted using laboratory tests, vital signs, and monitoring of adverse events. Economic evaluations will be conducted using either cost-minimization analysis or cost-utility analysis.

DISCUSSION

This trial will evaluate the efficacy, safety, and cost-effectiveness of CSBHT as an add-on therapy to LTRAs to establish its potential as an adjuvant therapy in asthma management.

TRIAL REGISTRATION

This study was registered in the Clinical Research Information Service of Korea (KCT0006005), on March 16, 2021.

摘要

背景

哮喘是一种以气道炎症和阻塞为特征的慢性疾病。治疗旨在使用控制疾病和缓解症状的药物,以最少的药物控制症状。吸入性类固醇和β2受体激动剂是常见的治疗方法;然而,长期使用它们可能会引起副作用。白三烯受体拮抗剂(LTRAs)因其抗炎和支气管扩张作用,与吸入性类固醇联合用于治疗哮喘。将LTRAs与韩国传统药物Chungsangboha-tang(CSBHT)联合使用可能会增强其疗效。本研究旨在通过一项随机、安慰剂对照、双盲、多中心临床试验,评估CSBHT作为哮喘辅助治疗方法的潜力。

方法

这项随机、安慰剂对照、双盲、平行组、多中心研究旨在评估CSBHT作为哮喘患者(尤其是使用LTRAs的患者)附加治疗的疗效和安全性。总共198名参与者将被随机分为干预组和对照组,前者每天服用三次CSBHT,后者服用安慰剂。在第0、4和8周的随访将包括结果测量、药物配发和不良反应监测。主要结果是一秒用力呼气量评分的平均变化,次要结果包括呼气峰值流速、用力肺活量、25%-75%用力呼气流量、呼出一氧化氮分数、哮喘控制测试、哮喘生活质量问卷、血清IgE、嗜酸性粒细胞计数、C反应蛋白、急救药物使用情况,以及对韩国传统医学哮喘症状问卷的描述性分析。将通过实验室检查、生命体征和不良事件监测进行安全性评估。将使用成本最小化分析或成本效用分析进行经济学评估。

讨论

本试验将评估CSBHT作为LTRAs附加治疗的疗效、安全性和成本效益,以确定其作为哮喘辅助治疗方法的潜力。

试验注册

本研究于2021年3月16日在韩国临床研究信息服务中心注册(KCT0006005)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a97/11829457/5ff7651449f0/12906_2025_4799_Fig1_HTML.jpg

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