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临床试验/NCT02824523
NCT02824523已完成不适用

Role of PDG2 in the Aspirin-Induced Reactions and in the Treatment of Aspirin-Exacerbated Respiratory Disease

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Therapeutic efficacy of high-dose aspirin as assessed by change in sinus symptoms (Sino-Nasal Outcome Test)

研究概览

简要总结

The purpose of this research study is to learn new information about the underlying cause of aspirin-exacerbated respiratory disease (AERD) and the benefit of high-dose aspirin therapy. AERD is a disease that involves asthma, recurring nasal polyps, and respiratory reactions to aspirin and other nonsteroidal anti-inflammatory drugs. This study will be conducted on individuals with AERD who are referred to the Brigham and Women's Hospital AERD Center for clinical evaluation and potential aspirin desensitization. Desensitization to aspirin and subsequent treatment with daily high-dose oral aspirin is standard of care for patients with AERD who do not respond adequately to steroids and have recurrent nasal polyposis or symptomatic asthma. This study will involve five visits to Brigham and Women's Hospital and will align closely with the standard of care for the treatment of AERD.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • History of asthma
  • History of nasal polyposis
  • History of at least one clinical reaction to oral aspirin or other nonselective COX inhibitor with features of both lower (cough, chest tightness, wheezing, dyspnea) and upper (rhinorrhea, sneezing, nasal obstruction, conjunctival itching and discharge) airway involvement
  • Stable asthma (post-bronchodilator FEV1 of ≥70%, no use of oral or systemic steroids for at least 1 month, and no hospitalizations or emergency room visits for asthma for the prior 6 months) at the time of entry into the study
  • Currently taking montelukast as part of standard asthma treatment for at least 4 weeks before the V1 visit
  • Exclusion criteria:
  • Pregnancy or current breastfeeding
  • History of bleeding diathesis or use of anticoagulant or antiplatelet drugs
  • History of thrombocytopenia < 50 x 10^9/L
  • Hypersensitivity to montelukast
  • Peptic ulcer disease
  • Unstable asthma (post-bronchodilator FEV1 of less than 70%, use of oral or systemic steroids for at least 1 month prior to visit 1, or hospitalizations or emergency room visits for asthma for the prior 6 months)
  • Use of zileuton (which can mask symptoms of aspirin-induced reaction) within 1 month prior to the V1 visit
  • Age under 18 or over 75 years
  • Current smoking

排除标准

  • 未提供

研究组 & 干预措施

High-dose aspirin

干预措施: aspirin (Drug)

结局指标

主要结局

Therapeutic efficacy of high-dose aspirin as assessed by change in sinus symptoms (Sino-Nasal Outcome Test)

时间窗: 8 weeks

Therapeutic efficacy of high-dose aspirin as assessed by asthma symptom control (Asthma Control Questionnaire)

时间窗: 8 weeks

Therapeutic efficacy of high-dose aspirin as assessed by change in lung function

时间窗: 8 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Tanya Laidlaw, MD

Associate Physician

Brigham and Women's Hospital

研究点 (1)

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