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.

IF 3.4 2区 医学 Q1 INTEGRATIVE & COMPLEMENTARY MEDICINE BMC Complementary Medicine and Therapies Pub Date : 2025-02-14 DOI:10.1186/s12906-025-04799-w
Sung-Woo Kang, Hae-Seong Nam, Yang-Chun Park, Jun-Yong Choi, Ki-Tae Kim, Seo-Jung Ha, Kwan-Il Kim, Hee-Jae Jung, Beom-Joon Lee
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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.

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白三烯受体拮抗剂和Chungsangboha-tang在哮喘患者中的附加治疗效果:一项随机、安慰剂对照、平行、多中心试验的方案。
背景:哮喘是一种以气道炎症和阻塞为特征的慢性疾病。治疗的目的是用最少的药物控制症状,使用控制疾病和缓解症状的药物。吸入类固醇和β 2激动剂是常见的治疗方法;然而,长期使用会产生副作用。白三烯受体拮抗剂(LTRAs)由于其抗炎和支气管扩张作用而与吸入类固醇联合使用来治疗哮喘。将LTRAs与韩国药物忠尚保荷汤(cshbht)联合使用,可以提高其疗效。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cshbht作为哮喘辅助治疗的潜力。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cshbht作为哮喘患者,特别是ltra患者额外治疗的有效性和安全性。总的来说,198名参与者将被随机分为干预组和对照组,前者每天接受三次cshbht,后者接受安慰剂。第0、4和8周的随访将包括结果测量、药物分配和不良反应监测。主要终点是用力呼气量在1秒评分中的平均变化,次要终点包括呼气峰流量、用力肺活量、用力呼气流量25-75%、呼气一氧化氮分数、哮喘控制试验、哮喘生活质量问卷、血清IgE、酸性粒细胞计数、c反应蛋白、抢救药物使用以及韩医哮喘症状问卷的描述性分析。安全性评估将通过实验室测试、生命体征和不良事件监测进行。将使用成本最小化分析或成本效用分析进行经济评价。讨论:本试验将评估cshbht作为LTRAs辅助治疗的疗效、安全性和成本效益,以确定其作为哮喘治疗辅助治疗的潜力。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(KCT0006005)注册。
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来源期刊
BMC Complementary Medicine and Therapies
BMC Complementary Medicine and Therapies INTEGRATIVE & COMPLEMENTARY MEDICINE-
CiteScore
6.10
自引率
2.60%
发文量
300
审稿时长
19 weeks
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