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临床试验/NCT07067541
NCT07067541已完成不适用

Clinical Observation of Topical Lidocaine Cream Combined With Moisturizing Cream in the Treatment of Atopic Dermatitis

First Affiliated Hospital of Kunming Medical University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2023年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
25
试验地点
1
主要终点
change in SCORAD (SCORing Atopic Dermatitis) from baseline

研究概览

简要总结

Twenty-five patients with atopic dermatitis applied lidocaine cream plus a moisturizer to the right limb and lidocaine cream alone to the left limb, twice daily for four weeks.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female patients aged 18-65 years.
  • Clinical diagnosis of atopic dermatitis according to the 2020 Guidelines for the Diagnosis and Treatment of Atopic Dermatitis in China (symmetrical eczematous lesions for ≥6 months plus personal/family atopy history or elevated IgE/eosinophilia).
  • Voluntarily signed informed consent form.

排除标准

  • Active heart, liver, kidney, or other serious systemic illness.
  • History of viral or bacterial infection within 1 month prior to enrollment.
  • Immunocompromised patients or those receiving systemic immunosuppressive therapy.
  • Known allergy to lidocaine, moisturizer components, or any study-related topical agents.
  • Pregnant or breastfeeding women.
  • Use of topical corticosteroids or calcineurin inhibitors within 2 weeks prior to enrollment.

研究组 & 干预措施

Control Group

Active Comparator

干预措施: Control lidocaine cream (Drug)

Experimental group

Experimental

干预措施: Experimental lidocaine cream + moisturizer cream (Drug)

结局指标

主要结局

change in SCORAD (SCORing Atopic Dermatitis) from baseline

时间窗: 4 weeks

For each patient, a score will be obtained at baseline, after 4 weeks. The minimum score is 0 (best outcome) and the maximum score is 103 (worst outcome).

次要结局

未报告次要终点

研究者

发起方
First Affiliated Hospital of Kunming Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tang Junting

Director

First Affiliated Hospital of Kunming Medical University

研究点 (1)

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