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临床试验/ITMCTR2000003561
ITMCTR2000003561尚未招募未知

A superiority designed study of Uygur medicine Luo-Ou-Ke Zu-Pa and Chinese medicine Xiao-Qing-Long-Tang Decoction in the treatment of cold asthma

Huashan Hospital Affiliated to Fudan University0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
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
18 至 75(—)
性别
All

入选标准

  • 1. Aged 18-75 years old at the time of enrollment;
  • 2. Patients with bronchial asthma diagnosed by modern medicine, regular inhaled hormone therapy or other conventional treatment 3 months later, patients with bronchial asthma ACT score <20 points;
  • 3. Patients with abnormal mucus type identified by Uighur medicine;
  • 4. Patients without upper and lower respiratory tract infections and not taking oral and intravenous glucocorticoid therapy within 2 weeks;
  • 5. Subjects voluntarily participated in the study and signed Informed consent.

排除标准

  • 1. Patients in acute attack stage, who need oral and intravenous glucocorticoid therapy;
  • 2. Patients with abnormal blood type, abnormal savda type, and abnormal biliary type identified by Uygur medicine;
  • 3. Combined Patients with COPD, pulmonary fibrosis, and a history of lung resection;
  • 4. Pregnant or planning to become pregnant or breastfeeding women;
  • 5. Patients with malignant tumors and hematological diseases;
  • 6. Those who have participated in clinical trials of other drugs within 3 months;
  • 7. Those with severe impairment of heart, liver, and kidney functions (heart function grades 3 to 4, ALT and/or AST exceeding 1.5 times the upper limit of normal, and Cr exceeding the upper limit of normal);
  • 8. Those deemed unsuitable for inclusion by the investigator Other situations.

研究者

发起方
Huashan Hospital Affiliated to Fudan University

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