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Efficacy and safety of fire needle therapy in treating non-segmental stable vitiligo: A randomized self-controlled clinical trial.
Wang, Yuyi; Lin, Mao; Huang, Fang; Jia, Ruiling; Xu, Wei; He, Qi; Xiong, Qiong; Hu, Qin; Diao, Qingchun; Liu, Zhaolan.
Afiliação
  • Wang Y; Centre for Evidence Based Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
  • Lin M; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • Huang F; Department of Dermatology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
  • Jia R; Chongqing Jiulongpo District Shiqiaopu Community Health Service Center, Chongqing, China.
  • Xu W; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • He Q; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • Xiong Q; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • Hu Q; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • Diao Q; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
  • Liu Z; Department of Dermatology, Chongqing Hospital of Traditional Chinese Medicine, Chongqing, China.
J Cosmet Dermatol ; 2024 Jun 18.
Article em En | MEDLINE | ID: mdl-38894565
ABSTRACT

BACKGROUND:

Vitiligo remains a challenging condition to treat. Fire needle therapy, a traditional Chinese medicine technique, has potential as an alternative therapeutic strategy. However, rigorous evidence on its efficacy is lacking.

OBJECTIVE:

We aimed to evaluate the efficacy and safety of fire needle therapy, alone and combined with topical tacrolimus ointment, for non-segmental stable vitiligo.

METHODS:

In this 6-month randomized self-controlled trial, 35 vitiligo patients were enrolled, providing three similar lesions each. Lesions were randomly allocated to receive fire needle monotherapy, 0.1% tacrolimus ointment monotherapy, or combined fire needle and tacrolimus ointment therapy. The main outcome was change in vitiligo surface area.

RESULTS:

In total, 29 patients completed the 6-month follow-up. The combination therapy group showed significantly greater reductions in vitiligo surface area compared to monotherapy groups starting at months 4 and 5. By the end of the study, combination therapy resulted in remarkably higher repigmentation responses, with 89.7% of lesions showing at least mild (≥25%) repigmentation and 51.7% showing good (≥50%) repigmentation. This significantly exceeded the outcomes with topical tacrolimus ointment alone, which only achieved 6.9% mild response and 6.9% good response. Fire needle monotherapy also demonstrated steady repigmentation over time, with 69% of lesions attaining a mild response by month 6. Importantly, no major adverse events occurred.

CONCLUSION:

This study provides promising preliminary evidence supporting the use of fire needle therapy, alone or in combination with topical tacrolimus ointment, for inducing repigmentation in non-segmental stable vitiligo. As a non-pharmacological approach, fire needle therapy warrants further study as an alternative vitiligo treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article