ITMCTR2200005679尚未招募2 期
A randomized controlled trial of Guben Qushi Huayu Decoction Combined with Shenling Baizhu powder in the treatment of psoriasis with spleen deficiency and dampness obstruction syndrome
Guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 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 70（—）
- 性别
- All
入选标准
- •1.The age is 18-70 years old, both male or female; 2.The patients who meet the diagnostic criteria of stable plaque psoriasis; 3.The degree of skin lesions was moderate (3 = PASI < 10 or 3% = BSA < 10%); 4.The patients who meet the diagnostic criteria of dampness syndrome; 5.Patients with informed consent.
排除标准
- •1.Drip type, reverse type, joint type, pustular type, erythrodermic psoriasis, or psoriasis vulgaris in progressive stage and regression stage. 2.Pregnant or lactating women, or those planning pregnancy within 1 year. 3.Patients with severe primary diseases such as respiratory system, circulatory system, digestive system, endocrine system and urinary system, which can not be controlled by conventional drugs; Patients with severe infection, hepatitis, pulmonary tuberculosis, lymphocyte proliferation, abnormal hematopoietic system and tumor; Patients with severe disorders of water, electrolyte and acid-base balance; Patients with primary or secondary immunodeficiency and hypersensitivity; Or patients whose clinical test indexes belong to one of the following situations: the increase of alanine aminotransferase or aspartate aminotransferase > 1.5 times the upper limit of normal value; The increase of creatinine > 1.5 times the upper limit of normal value; Hemoglobin increase > 20g / L, upper limit of normal value; Thrombocytopenia < 75.0 × 10e9/L Decrease in leukocyte count < 3.0 × 10e9/L The increase of blood potassium is more than 5.5mmol/l or the decrease is less than 3mmol / L, or other abnormal laboratory tests. The researchers judge that it is not suitable for patients to participate in this test. 4.Patients who are known to be allergic to the drugs used in this study and those containing related drug components. 5.Those who are participating in other drug clinical trials or have participated in other clinical trials within 1 month. 6.Patients considered unsuitable for inclusion by the researchers.
研究者
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