跳至主要内容
临床试验/NCT07331792
NCT07331792尚未招募1 期

Comparative Efficacy of Topical 1% Clotrimazole vs Oral Itraconazole in the Treatment of Pityriasis Versicolor

Combined Military Hospital Abbottabad0 个研究点目标入组 86 人开始时间: 2026年2月2日最近更新:
干预措施

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
86
主要终点
Percentile efficacy of topical versus oral antifungal in the treatment of pityriasis versicolor

研究概览

简要总结

Comparative efficacy of topical 1% clotrimazole vs oral itraconazole in the treatment of pityriasis versicolor -Randomized control trial

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 (Participant)

入排标准

年龄范围
15 Years 至 50 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Age (15-50 years)
  • Both genders
  • Sufferers of Pityriasis versicolor ( Determined by scale , erythema and pruritus)

排除标准

  • Pt with history of antifungals in last one month
  • Pt on immunosuppressants or steroid therapy
  • Pregnant and lactating women
  • Pt with chronic medical conditions ( Diabetes and hypertension)

研究组 & 干预措施

1% Clotrimazole

Experimental

topical 1 % clotrimazole twice daily for 2 weeks

干预措施: Topical 1 % clotrimazole twice daily 2 weeks (Drug)

Itraconazole

Experimental

Oral itraconazole 200mg daily 5 days

干预措施: Oral itraconazole 200mg daily for 5 days (Drug)

结局指标

主要结局

Percentile efficacy of topical versus oral antifungal in the treatment of pityriasis versicolor

时间窗: 3 months

Data analysis will be performed using SPSS version 20. The quantitative variable (age, BMI and duration of PV) will be presented as mean ± standard deviation (SD) or median interquartile range (IQR) after checking normality of data by using Shapiro-Wilk test. Frequency and percentages will be used for categorical variables (gender, severity of PV, area of residence, level of education and efficacy). Efficacy will be compared between groups using Chi-square or Fisher exact test. Efficacy will be stratified by age, gender, BMI, duration of PV and severity of PV to deal with effect modifiers. Post-stratification chi-square test or Fischer exact test will be used as test of significance. A p-value of ≤ 0.05 will be considered statistically significant.

次要结局

未报告次要终点

研究者

发起方
Combined Military Hospital Abbottabad
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zaeema Aman

Resisent Dermatology

Combined Military Hospital Abbottabad

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