ITMCTR2100004855
Recruiting
Phase 1
A randomized, double-blind, controlled study on the treatment of stable vitiligo with compound Honghuabuji granules
Shanghai Dermatology Hospital0 sitesTBD
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Shanghai Dermatology Hospital
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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