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临床试验/ITMCTR1900002670
ITMCTR1900002670
尚未招募
1 期

A randomized controlled trial for prevention of acute exacerbation of stable Chronic Obstructive Pulmonary Disease with acupoint application of traditional Chinese medicine

Hospital of Chengdu University of Traditional Chinese Medicine0 个研究点待定

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Chronic Obstructive Pulmonary Disease
发起方
Hospital of Chengdu University of Traditional Chinese Medicine
状态
尚未招募
最后更新
3年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
3年前
研究类型
Interventional study
性别
All

研究者

发起方
Hospital of Chengdu University of Traditional Chinese Medicine

入排标准

入选标准

  • 1\. Age ranged from 45 to 70 years, male or female.
  • 2\. In accordance with the COPD diagnostic criteria in the GOLD guidelines, and GOLD 2 to 3: FEV1/FVC \<70% and 30% predicted value \<\= FEV1\< 80% predicted value in 20 minutes after inhalation of salbutamol 400ug.
  • 3\. The patient is in a stable phase of COPD: the patient's symptoms such as cough, sputum, and shortness of breath are stable or mild, and the condition is basically restored to the state before acute exacerbation.
  • 4\. Patients with spleen\-lung qi deficiency syndrome that meet the diagnostic criteria for common syndrome of traditional Chinese medicine.
  • 5\. Subjects volunteer to participate in the study and sign an informed consent form.

排除标准

  • 1\. Combined with chronic lung diseases requiring intervention or treatment such as bronchial asthma,interstitial lung disease, active tuberculosis, bronchiectasis.
  • 2\. Combined with severe primary diseases such as severe mental disorders, cardiovascular and cerebrovascular diseases, liver and kidney diseases, endocrine diseases, hematopoietic system diseases, malignant tumors, etc.
  • 3\. There were skin wounds, skin ulcers and skin infections on the application site.
  • 4\. Those who are allergic to traditional Chinese medicine, excipients or dressings for the project.
  • 5\. Patients with limited limb movements.
  • 6\. Women who are breastfeeding, pregnant or preparing for pregnancy.
  • 7\. Participated in other clinical studies in the past six months.

结局指标

主要结局

未指定

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