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首页> 外文期刊>BMJ Open >Early intervention with tiotropium in Chinese patients with GOLD stages I–II chronic obstructive pulmonary disease (Tie-COPD): study protocol for a multicentre, double-blinded, randomised, controlled trial
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Early intervention with tiotropium in Chinese patients with GOLD stages I–II chronic obstructive pulmonary disease (Tie-COPD): study protocol for a multicentre, double-blinded, randomised, controlled trial

机译:噻托溴铵对中国GOLD I–II期慢性阻塞性肺疾病(Tie-COPD)患者的早期干预:一项多中心,双盲,随机对照研究的研究方案

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Introduction Owing to the high and increasing morbidity and mortality, chronic obstructive pulmonary disease (COPD) has become a major public health problem worldwide. Although the majority of patients with COPD are in the early stages, little attention has been paid to them, in particular regarding to early intervention. Tiotropium bromide can significantly relieve symptoms and reduce the incidence of acute exacerbations of COPD. Therefore, we hypothesise that therapy with tiotropium bromide will benefit patients with COPD with early-stage disease. Method/analysis A randomised, double-blinded, placebo-controlled, parallel-group, multicentre clinical trial (Tiotropium In Early COPD study, Tie-COPD study) is being conducted to evaluate the efficacy and safety of long-term intervention with tiotropium in patients with COPD with early-stage disease. A total of 839 patients with COPD who satisfied the eligibility criteria were randomly assigned (1:1) to receive a once daily inhaled capsule of either tiotropium bromide (18?μg) or matching placebo for 2?years. Measurements will include forced expiratory volume in 1?s, health-related quality of life, grade degree of breathlessness related to activities, COPD exacerbations and pharmacoeconomic analysis. Ethics/dissemination This study was approved by the Ethics Committee of the First Affiliated Hospital of Guangzhou Medical University. Recruitment started in November 2011 and ended in October 2013, with 839 patients randomised. The treatment follow-up of participants with Tie-COPD is currently ongoing and is due to finish in November 2015. The authors will disseminate the findings in peer-reviewed publications, conferences and seminar presentations. Trial registration ClinicalTrials.gov (NCT01455129).
机译:引言由于高发病率和高死亡率,慢性阻塞性肺疾病(COPD)已成为世界范围内的主要公共卫生问题。尽管大多数COPD患者处于早期阶段,但对其关注很少,特别是在早期干预方面。噻托溴铵可显着缓解症状并减少COPD急性加重的发生率。因此,我们假设噻托溴铵疗法将使患有早期疾病的COPD患者受益。方法/分析正在进行一项随机,双盲,安慰剂对照,平行组,多中心的临床试验(噻托溴铵在早期COPD研究中,Tie-COPD研究),以评估长期使用噻托溴铵治疗的有效性和安全性。患有早期疾病的COPD患者。总共839名符合入选条件的COPD患者被随机分配(1:1)接受噻托溴铵(18?μg)或匹配安慰剂的每日一次吸入胶囊治疗2年。测量将包括1秒内的呼气量,与健康有关的生活质量,与活动有关的呼吸困难等级,COPD恶化和药物经济学分析。伦理/传播本研究得到广州医科大学附属第一医院伦理委员会的批准。招募始于2011年11月,结束于2013年10月,随机分配了839名患者。 Tie-COPD参与者的治疗随访目前正在进行中,预计于2015年11月完成。作者将在同行评审的出版物,会议和研讨会演示中传播研究结果。试用注册ClinicalTrials.gov(NCT01455129)。

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