跳至主要内容
临床试验/CTRI/2025/05/086402
CTRI/2025/05/086402尚未招募不适用

To study effectiveness of Fractional CO2 laser therapy combined with 8%Cicloprix Nail Lacquer versus Q switched Nd YAG laser combined with 8% Cicloprix Nail Lacquer in the treatment of Onychomycosis using a split side design within the same individual. A pilot study.

Institute of Naval Medicine, INHS Asvini, Mumbai1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年5月17日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
clinical efficacy and clinical cure rates of fractional CO2 laser therapy and Q switched Nd YAG laser therapy combined with 8% ciclopirox nail lacquer in reducing fungal nail infection symptoms.

研究概览

简要总结

Comparing Fractional CO2 laser vs Nd YAG laser in thetreatment of Onychomycosis along with topical 8% ciclopirox nail lacquer

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 18 to 60 years of age Positive KOH microscopy Treatment naive patients.

排除标准

  • Age below 18 years and more than 60 years In the case of female subjects, are pregnant, nursing or planning to become pregnant within the study period Individuals with negative KOH mounts Presence of other diseases causing nail dystrophy such as psoriasis, eczema, and lichen planus and immunodeficiency such as HIV infected patients, patients with organ transplantation and currently on immunosuppressive drugs for long periods or patients under chemotherapy or radiotherapy Any significant disease of the hepatic, renal, endocrine including diabetes mellitus, immune systems, or other health conditions which could interfere with or confound the results of study assessments, pre existing chronic foot pain, neurologic deficit or skin disease or injury in treated foot.

结局指标

主要结局

clinical efficacy and clinical cure rates of fractional CO2 laser therapy and Q switched Nd YAG laser therapy combined with 8% ciclopirox nail lacquer in reducing fungal nail infection symptoms.

时间窗: 04 months

次要结局

  • evaluate patient-reported outcomes including pain, discomfort, and cosmetic improvement.(04 months)

研究者

发起方
Institute of Naval Medicine, INHS Asvini, Mumbai
申办方类型
Research institution and hospital

研究点 (1)

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