研究疾病:
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小气道病变
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研究疾病代码:
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Target disease:
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Small Airway Disease
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Target disease code:
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研究类型:
Study type:
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干预性研究
Interventional study
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研究设计:
Study design:
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随机平行对照
randomized controlled trial(parallel group design)
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研究所处阶段:
Study phase:
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探索性研究/预试验
Pilot clinical trial
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研究目的:
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探索性研究止嗽散对小气道病变患者肺功能和生物炎症标志物的影响,为临床上使用止嗽散治疗小气道病变提供参考依据。
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Objectives of Study:
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To explore on the effect of Zhisou Powder on pulmonary function and bio-inflammatory markers in patients with small airway disease,provides a reference for clinical using of Zhisou Powder to treat this diseases.
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药物成份或治疗方案详述:
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止嗽散由紫菀(蒸) 、百部(蒸)、桔梗(炒)、白前(蒸)、荆芥、陈皮(水洗去白)、甘草(炒)组成。
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Description for medicine or protocol of treatment in detail:
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Zhisou Powder is composed of Aster tataricus (steamed), Stemona japonica (steamed), Platycodonis Radix (stir-fried), Cynachi Stauntonii Rhizoma EtRadix (steamed), Fineleaf Schizonepeta Herb, Citri Reticulatae Pericarpium (washed to remove white), and Glycyrrhiza Uralensis Fisch (stir-fried).
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纳入标准:
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①年龄:18岁及其以上,男、女不限。
②符合小气道病变的肺功能标准:MMEF、FEF50、FEF75下降,多于2项指标低于65%预计值。
③愿意口服中药治疗。
④能进行语言或文字交流书写能力。
⑤自愿签署知情同意书。
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Inclusion criteria
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1. More than 18 years old, male or female;
2. Meet the pulmmonary function criteria for small airway disease: MMEF, FEF50, FEF75 decreased, and more than 2 indicators were lower than 65% of the expected value;
3. Willing to take oral Chinese medicine treatment;
4. Able to communicate and write in language or text;
5. Sign the informed consent form voluntarily.
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排除标准:
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①存在重大疾病,如肺部恶性肿瘤、心功能不全、肾功能衰竭、痴呆、癫痫、活动性肺结核等。
②近1周内使用呼吸系统药物,如吸入用糖皮质激素、抗胆碱能药物、β2受体激动剂、白三烯受体拮抗剂等。
③现处于呼吸道疾病急性加重期,如慢阻肺急性加重期,哮喘急性发作期等。
④既往3个月内急性心脑血管事件(中风、短暂性脑缺血发作、急性冠脉综合征)。
⑤未完全治愈的恶性肿瘤史。
⑥精神疾病、药物成瘾或酗酒。
⑦哺乳期、妊娠期或近期计划妊娠。
⑧中药材过敏史,或不愿意口服中药制剂。
⑨预计不能配合,或不适于随访者。
⑩未签知情同意书。
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Exclusion criteria:
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1. There are major diseases, such as lung malignant tumors, heart failure, renal failure, dementia, epilepsy, active tuberculosis, etc.;
2. Using respiratory drugs in past weeks,such as inhaled corticosteroids, anticholinergic drugs, β2 receptor agonists, leukotriene receptor antagonists, etc.;
3. Currently in acute exacerbation of respiratory diseases, such as acute exacerbation of chronic obstructive pulmonary disease, acute exacerbation of asthma, etc.;
4. Acute cardiovascular and cerebrovascular events (stroke, transient ischemic attack, acute coronary syndrome) in the past 3 months;
5. History of malignant tumors that are not completely cured;
6. Mental illness, drug addiction or alcoholism;
7. Lactation, pregnancy, or planned pregnancy in the near future;
8. History of allergy to Chinese medicinal materials, or unwillingness to take Chinese medicinal preparations;
9. Those who are not expected to cooperate or are not suitable for follow-up;
10. The informed consent is not signed.
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研究实施时间:
Study execute time:
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从From
2021-01-01
至To
2022-12-31
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征募观察对象时间:
Recruiting time:
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从From
2021-01-01
至To
2022-12-31
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