ITMCTR2100004855招募中1 期
A randomized, double-blind, controlled study on the treatment of stable vitiligo with compound Honghuabuji granules
Shanghai Dermatology Hospital0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 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 60(—)
- 性别
- All
入选标准
- •1. Patients who are clearly diagnosed as vitiligo, and those who have been diagnosed as blood stasis syndrome by Chinese medicine;
- •2. Patients aged 18 to 60 years;
- •3. Mainly confined and sporadic;
- •4. In order to accurately compare the test results, the hypopigmented area of all patients in this test is <= 10% of the total body surface area;
- •5. No systemic or topical glucocorticoid or immunosuppressant treatment or withdrawal of the drug for more than 3 months within 3 months;
- •6. Patients with leukoplakia that have not expanded within 6 months and are in a stable phase;
- •7. Patients who agree to take pictures of the skin lesions and can complete the treatment and follow-up on time.
排除标准
- •1. Pregnant and lactating women;
- •2. System or topical vitiligo drug treatment within 3 months;
- •3. Patients who are allergic to tacrolimus ointment and compound Honghuabuji granules.
- •4. Patients with severe heart, liver, kidney and other system diseases;
- •5. Patients who withdraw halfway and have incomplete information.
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