The Study About the Identification of Treatable Traits of Severe Asthma and the Construction of Personalized Treatment System
报名条件(概要)
- 年龄:18 Years – 80 Years
- 性别:不限
- 健康志愿者:不接受
完整入排标准请以官方页面为准。
开展国家/地区
China
药品与企业信息
Individualized cluster management for treatable traits
Routine asthma treatment according to current guidelines
研发企业
试验官方登记的主要申办方;研究机构申办时会显示相应机构名称。
生产企业
公开药品批准资料或正式说明书暂未提供明确的生产企业信息。
合作机构
- Second Affiliated Hospital, Zhejiang University, School of Medicine研究机构/其他
- The First Affiliated Hospital of Guangzhou Medical University研究机构/其他
- Shanxi Bethune Hospital研究机构/其他
- Henan Provincial People's Hospital研究机构/其他
- First Hospital of China Medical University研究机构/其他
- China-Japan Friendship Hospital研究机构/其他
- Beijing Tiantan Hospital研究机构/其他
- Second Xiangya Hospital of Central South University研究机构/其他
- Ruijin Hospital研究机构/其他
研发企业与生产企业可能不是同一家。研究阶段药品可能尚未公布生产企业;生产企业仅取自美国上市原研药说明书所列企业(不含仿制药),不作推测;仅在其他国家上市的药品暂无法显示。
研究简介(原文)
Severe asthma is a complex and heterogeneous disease. Patients with severe asthma can present with different types of airway inflammation, and are often accompanied by a variety of comorbidities and risk factors. Identification of potentially modifiable factors affecting prognosis, that is, "treatable characteristics", and individualized bundle management based on these characteristics may help to improve the quality of life of patients with asthma and improve the level of asthma control. Through joint research, this project aims to evaluate the treatable characteristics of asthma in patients with severe asthma in tertiary hospitals across the country, including lung function, fractional exhaled nitric oxide, blood routine, allergen IgE, chest CT, and a detailed questionnaire. The distribution of treatable characteristics of patients with severe asthma and its impact on the quality of life or asthma control level of patients were investigated. For patients with severe asthma, multidisciplinary consultation and shared decision-making were used to establish an individualized bundle management model based on the treatable characteristics of severe asthma. A 6-month randomized parallel controlled clinical trial was conducted to determine whether this model was superior to conventional management in improving the quality of life or asthma control in patients with severe asthma. The implementation of this project will build a new model of individualized management of severe asthma based on treatable characteristics and improve the management level of severe asthma
适应症
主动联系研究团队
总联系人(申办方/研究总部)
- Kewu Huang, professorkewuhuang@126.com8613601234681
中国/港澳台研究中心
- Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical UniversityBeijing,Beijing Municipality,China
- Beijing Tiantan Hospital Affiliated to Capital Medical UniversityBeijing,Beijing Municipality,China
- China-Japan Friendship HospitalBeijing,Beijing Municipality,China
- The First Affiliated Hospital of Guangzhou Medical UniversityGuangzhou,Guangdong,China
- Henan Provincial People's HospitalZhengzhou,Henan,China
- The Second Xiangya Hospital of Central South UniversityChangsha,Hunan,China
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英文版(发给研究团队)
Dear Study Team, I am a patient in China and I am interested in participating in your clinical trial: Study Title: The Study About the Identification of Treatable Traits of Severe Asthma and the Construction of Personalized Treatment System ClinicalTrials.gov Identifier: NCT07136025 Sponsor: Beijing Chao Yang Hospital Investigational product: Individualized cluster management, Routine asthma treatment About me: - Age: (please fill in) - Sex: (please fill in) - Confirmed diagnosis and stage: (please fill in) - Biomarkers / genetic testing: not available - Prior and current treatments: (please fill in) - Performance status (ECOG): not assessed - Current location: China - Travel ability: (please fill in) Could you please let me know: 1. Whether I might be eligible for this study; 2. Which site would be closest and most practical for me, and whether remote pre-screening is possible; 3. What documents (medical records, pathology or imaging reports, recent labs) I should prepare for pre-screening. I can provide English translations of my medical records. Thank you very much for your time and help. Kind regards, (your name) (your email / phone with country code)
中文对照(供您核对)
尊敬的研究团队: 我是一位来自中国的患者,希望咨询参加以下临床试验的可能: 研究名称:The Study About the Identification of Treatable Traits of Severe Asthma and the Construction of Personalized Treatment System 试验编号:NCT07136025 申办方:Beijing Chao Yang Hospital 研究药物:Individualized cluster management、Routine asthma treatment 我的基本情况: - 年龄:(请填写) - 性别:(请填写) - 确诊疾病与分期:(请填写) - 基因/标志物检测:暂无 - 既往及当前治疗:(请填写) - 体能状态(ECOG):未评估 - 目前所在城市:中国 - 可前往范围:(请填写) 想请教三个问题: 1. 我是否可能符合本研究的入组标准? 2. 哪个中心对我最方便可行?能否远程预筛? 3. 预筛需要准备哪些资料(病历、病理、影像、近期化验)? 我可以提供英文翻译版病历。感谢您的时间与帮助。 顺祝安康 (您的姓名) (您的邮箱/带国际区号的电话)
提示:请与主治医生一起发信——由医生署名的申请,回复率远高于患者单独发信。首封邮件不要附身份证号等敏感信息。研究团队通常在 3–10 个工作日内回复,两周无回音可礼貌追问一次。
下一步怎么做?
- 把本页信息带给您的主治医生,评估是否适合参加。
- 点击下方按钮打开官方注册页,查看研究中心联系方式。
- 直接联系研究团队咨询报名事宜(通常有中文同声翻译服务可协助沟通)。