跳至主要内容
临床试验/NCT07329907
NCT07329907已完成2 期

Comparative Efficacy of Topical Salicylic Acid/Lactic Acid, Intralesional Candida Antigen, and Their Combination in the Treatment of Warts: A Randomized, Assessor-Blinded, Controlled Trial

Benha University1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2023年12月1日最近更新:
干预措施

试验速览

阶段
2 期
状态
已完成
入组人数
126
试验地点
1
主要终点
Complete Response (CR) Rate

研究概览

简要总结

Objective: To compare the efficacy, safety, and recurrence rates of topical salicylic acid/lactic acid (SA/LA) monotherapy (Group A), intralesional Candida antigen (CA) monotherapy (Group B), and their combination (Group C) for the treatment of warts.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Assessor-Blinded (Outcome Assessor Only)

入排标准

年龄范围
5 Years 至 60 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Single or multiple warts.
  • Aged 5 to 60 years.
  • Eligible for both topical and intralesional treatments.
  • No prior wart treatment for at least 1 month.

排除标准

  • Pregnancy or lactation.
  • Immunosuppression or use of immunosuppressive drugs.
  • Known sensitivity to study ingredients.
  • Systemic/local inflammation or infection.
  • History of bleeding/clotting disorder, or use of anticoagulants/NSAIDs.
  • History of asthma, allergic skin disorders, or convulsions.
  • History of chronic systemic diseases (renal/hepatic failure, cardiovascular disorders).

研究组 & 干预措施

Intralesional Monotherapy

Active Comparator

Patients receive intralesional injection of Candida Antigen (0.1-0.3 mL) every 2 weeks for up to 6 sessions.

干预措施: Candida Antigen Intralesional Injection (Biological)

topical monotherapy

Active Comparator

Patients receive topical application of Salicylic Acid 40% and Lactic Acid 16% once daily for up to 6 weeks.

干预措施: Salicylic Acid/Lactic Acid Topical Solution (Drug)

Combination Therapy

Active Comparator

Patients receive intralesional injection of Candida Antigen (0.1-0.3 mL) every 2 weeks for up to 6 sessions, with topical Salicylic Acid 40% and Lactic Acid 16% applied in between.

干预措施: Candida Antigen and Salicylic Acid/Lactic Acid (Combination Product)

结局指标

主要结局

Complete Response (CR) Rate

时间窗: 3 months post-treatment

Percentage of patients achieving complete disappearance of all warts.

次要结局

  • Safety and Tolerability Profile(At each visit (every 2 weeks) and 3 months post-treatment)
  • Recurrence Rate(6 months post-treatment)
  • Distant Wart Clearance Rate(3 months post-treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ghada Mohamed Shams

Principal investigator

Benha University

研究点 (1)

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