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Two Percentage of Ketoconazole Cream for the Treatment of Adult Female Acne: A Placebo-Controlled Trial

机译:两种百分比的酮康唑霜用于治疗成人女性痤疮:安慰剂对照试验

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Introduction Our objective was to determine the efficacy of ketoconazole (KTZ) 2% cream for the treatment of mild adult female acne (AFA). Materials and methods This placebo-controlled trial was conducted in District Headquarters (DHQ) Teaching Hospital, Sahiwal, Pakistan. The study was completed in a period of January 2019-June 2020. A total of 60 females of age 25 years having mild AFA were included. In Group I, the patients were advised to apply 2.0% KTZ cream covering the whole skin area twice daily for a period of eight weeks. In Group II (placebo group) patients, a topical cream containing propylene glycol was applied for similar period. After eight weeks, the cream was discontinued and participants were advised to use routine skincare products, and follow-up was done after two weeks. The main study outcome was reduction in the total count of acne lesions including both inflammatory and non-inflammatory lesions and overall success rate of treatment. Results Mean age was 36.2 ± 6.3 years in KTZ group versus 35.4 ± 6.5 years in control group. Mean duration of acne was 14.3 ± 7.3 years in KTZ group versus 15.1 ± 6.9 years in control group. Improvement in facial adult female acne scoring tool (AFAST) scale (AFAST-F) was observed in 13 (43.3%) patients in KTZ group and in only 4 (13.3%) patients in control group (p value = 0.009). Improvement in submandibular AFAST (AFAST-S) was observed in 12 (40.0%) patients in KTZ group and in eight (26.7%) patients in control group. The overall success rate of treatment was 14 (46.7%) in KTZ group versus 4 (13.3%) in control group (p value = 0.012). Conclusions In our study, we found significant improvement in reduction of acne lesions as well as complete recovery using 2.0% ketoconazole for the treatment of mild AFA. So KTZ can be used as a preferred treatment option for these patients.
机译:介绍我们的目标是确定酮康唑(KTZ)2%乳膏治疗轻度成人女性痤疮(AFA)的疗效。材料和方法本安慰剂对照试验在巴基斯坦Sahiwal教学医院(DHQ)教学医院进行。该研究在2019年1月20日至6月20日期间完成。包括60名年龄> 25岁的女性,其中25岁。在群体中,建议患者涂抹2.0%KTZ霜,每天两次覆盖整个皮肤区域,持续八周。在II族(安慰剂组)患者中,施用含丙二醇的局部乳霜相似。八周后,奶油已停产,建议参与者使用常规护肤品,并在两周后完成后续行动。主要研究结果减少了痤疮病变的总计数,包括炎症和非炎症病变和整体成功率治疗。结果平均年龄为36.2±6.3岁,对照组的35.4±6.5岁。痤疮的平均持续时间为KTZ组的14.3±7.3岁,对照组15.1±6.9岁。在KTZ组中的13例(43.3%)患者中观察到面部成年女性痤疮评分工具(AFAST-F)的改善,对照组仅为4名(13.3%)患者(P值= 0.009)。在KTZ组的12名(40.0%)患者中观察到颌下余量(AFAST-S)的改善,并在对照组中的八个(26.7%)患者中观察到。治疗总体成功率为14(46.7%)在KTZ组,对照组中4(13.3%)(P值= 0.012)。结论在我们的研究中,我们发现减少痤疮病灶的显着改善,以及使用2.0%酮康唑来治疗温和AFA的完全恢复。因此KTZ可用作这些患者的优选治疗选择。

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