ITMCTR2100004789
Recruiting
Phase 1
Clinical observation of fire needle combined with halometasone cream in the treatment of acral vitiligo
Dermatology Hospital,Southern Medical University0 sitesTBD
ConditionsVitiligo
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Vitiligo
- Sponsor
- Dermatology Hospital,Southern Medical University
- Status
- Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Meet the diagnostic criteria and consensus on diagnosis and treatment, meet the criteria for acral typing, meet the criteria for stable stage staging, and be stable for at least 6 months;
- •2\. Aged 18 to 60 years, gender is not limited, the course of disease is less than 5 years;
- •3\. There is no pigment island and self\-healing tendency in leukoplakia;
- •4\. The skin lesion area accounts for \<\= 1% of the body surface area;
- •5\. Have not received immunosuppressive agents, glucocorticoids, non\-steroidal anti\-inflammatory drugs and other systemic treatments within 3 months, and have not received local treatments within 1 month;
- •6\. Patients who agree to and abide by the diagnosis and treatment plan, voluntarily sign an informed consent form, and cooperate in taking photos before and after treatment.
Exclusion Criteria
- •1\. Fainted needles, scarred physique, or extremely fearful of fire needles;
- •2\. Patients who are allergic to halometasone cream;
- •3\. Patients with combined serious diseases, such as serious heart, brain, liver, kidney, hematopoietic system and other system diseases, or patients with malignant tumors;
- •4\. Female patients who are pregnant, breastfeeding or planning to become pregnant within six months;
- •5\. Partial skin lesions have redness, swelling, damage or infection.
Outcomes
Primary Outcomes
Not specified
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