The efficacy and safety of Fluticasone Furoate/Umeclidinium/vilanterol (FF/UMEC/VI) on cough symptoms in adult patients with asthma, a randomized double-blind, placebo-controlled, parallel group study: Chronic Cough in Asthma (COCOA) study.

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Tác giả: Tomohiro Akaba, Yasuhiro Aoki, Ryo Atsuta, Kaoru Chiba, Koichi Fukunaga, Yasuhiro Gon, Hisato Hiranuma, Masayuki Hojo, Soichiro Hozawa, Katsunori Masaki, Hiroyuki Nagase, Hiroyuki Ohbayashi, Jun Shinada, Naruhiko Sugihara, Etsuko Tagaya, Akihiko Tanaka, Junko Terada-Hirashima, Mayoko Tsuji, Osamitsu Yagi

Ngôn ngữ: eng

Ký hiệu phân loại: 069.50289 Collections and exhibits of museum objects

Thông tin xuất bản: England : The Journal of asthma : official journal of the Association for the Care of Asthma , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 752765

 BACKGROUND: Persistent cough bothers many patients with asthma because it worsens their quality of life
  therefore, it must be remedied immediately. The efficacy of triple therapy as a first-line treatment for cough remains unclear. To evaluate the effectiveness and safety of the triple therapy against persistent cough, the clinical effect of regular treatment with fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI) or placebo in adult patients with asthma was investigated. METHODS: This randomized, double-blind, placebo-controlled, parallel-group multicenter trial recruited asthma patients with persistent cough from hospitals and primary care clinics between June 2022 and December 2023. Participants were randomly given FF/UMEC/VI 200/62.5/25 µg or placebo for 6 wk. The primary endpoint was the average change in the cough symptom score from baseline to week 6. Secondary outcomes were effectiveness on cough-related disease burdens (asthma control questionnaire [ACQ]-5, Leicester cough questionnaire [LCQ] and nighttime awakening). Furthermore, lung function and adverse events were evaluated. RESULTS: The decrease from baseline in the cough symptom score at week 6 was significantly greater in the FF/UMEC/VI group than in the placebo group ( CONCLUSIONS: In asthma patients with persistent cough, FF/UMEC/VI showed an early response and a significant effect on cough and lung function for 6 wk of treatment. UNLABELLED: This study is registered with jRCTs031210412.
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