ITMCTR2000003400招募中1 期
Clinical efficacy evaluation of Qingda Granule in the treatment of hypertension (grade 1, low to medium-risk) patients: a multicenter, randomized, double-blind, double-simulated, parallel-controlled, non-inferiority clinical study
适应症
试验速览
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
- 20 至 75(—)
- 性别
- All
入选标准
- •1. Meet the diagnostic criteria for essential hypertension measured in the same clinic, the hypertension is graded as grade 1, and the risk stratification is low to medium risk (refer to the 2018 Revision of Chinese Guidelines for The Prevention and Treatment of Hypertension);
- •2. Did not take or did not take blood pressure medicine regularly within one month;
- •3. Between 20 and 75 years old (including boundary value);
- •4. Agree to sign the informed consent.
排除标准
- •1. Patients with obvious liver and kidney diseases or with ALT and AST 1.5 times higher than ULN, Cr and BUN higher than ULN;
- •2. Patients with serious mental illness, hematopoietic disease, malignant tumor and other major diseases;
- •3. Women who are pregnant or preparing for pregnancy, and women who are breastfeeding;
- •4. Have participated in or are participating in other clinical researchers in the past three months;
- •5. Suspected or definite allergy to the study drug.
研究者
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