ITMCTR2100005376尚未招募3 期
Efficacy and safety of Binafuxi granule in the treatment of common cold (heat syndrome): a multi-center, randomized, double-blind, placebo-controlled phase III clinical trial
West China Hospital, Sichuan University0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 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 65（—）
- 性别
- Male
入选标准
- •(1) Diagnosis of common cold according to Western medicine and symptom presenting within 48 hours;
- •(2) With fever and body temperature between 37.5 degree Celsius and 39 degrees Celsius;
- •(3) Diagnosis of common cold with heat syndrome according to traditional Uighur medicine;
- •(4) Aged between 18 and 65 years;
- •(5) Willing to participate and sign the informed consent.
排除标准
- •(1) Diagnosis of common cold with cold syndrome according to traditional Uighur medicine;
- •(2) Patients with influenza, acute or chronic rhinitis, acutel sinusitis, suppurative tonsillitis, pneumonia and Tuberculosis;
- •(3) white blood cell count>11.0 × 10^9/L and/or neutrophils percentae > 80%;
- •(4) Patients who are taking any medication to treat common cold;
- •(5) Patients with gastrointestinal discomfort symptoms such as acute and chronic diarrhea;
- •(6) Patients with serious primary diseases of the cardiovascular, pulmonary, kidney, liver, neurological and hematological system;
- •(7) Pregnant women, lactating women, or women who have a birth plan;
- •(8) Patients with allergic constitution or being allergic to the study drug;
- •(9) Patients who are participating in or have participated in another drug clinical trial within the last 3 months;
- •(10) Patients who have been judged by the investigator as inappropriate to participate in the clinical trial.
研究者
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