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临床试验/ITMCTR2000003210
ITMCTR2000003210招募中1 期

Effect of Jianpiyifei II granule on patients with mild to moderate Chronic Obstructive Pulmonary Disease (COPD): a randomized controlled clinical trial

Guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
40 至 85(—)
性别
All

入选标准

  • 1. Aged 40 to 85 years, both men and women;
  • 2. A diagnosis of mild to moderate COPD which defined by the GOLD Guidelines as post-bronchodilator FEV1/FVC <0.7 and FEV1 >= 50% predicted value;
  • 3. Stable COPD before screening, that is, no acute exacerbation at least 4 weeks prior to trial entry and no hospitalization for exacerbation in the past 3 months;
  • 4. TCM syndrome differentiation is Qi deficiency syndrome or Qi deficiency is the main syndrome;
  • 5. patients signed informed consent.

排除标准

  • 1. Had a history of asthma, bronchiectasis, lung cancer, active pulmonary tuberculosis and pneumonectomy;
  • 2. Experienced frequent acute exacerbations (>=3 times) of COPD in the past year;
  • 3. Had a blood eosinophil count >= 300/µL;
  • 4. Frequent oral or intravenous corticosteroids (prednisone >10 mg/day);
  • 5. TCM syndrome differentiation is excess syndrome and heat Syndrome;
  • 6. Those who are not willing to accept the observation measures or can not cooperate because of mental illness;
  • 7. Those who cannot complete the lung function test;
  • 8. Those who took herbal medicines for strengthening the spleen and benefiting the lungs two weeks before the trial, or those who had undergone lung rehabilitation within three months, or planned to undergo lung rehabilitation during the study.

研究者

发起方
Guangdong Provincial Hospital of Chinese Medicine

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