首页> 外文期刊>International journal of STD & AIDS >An open-label phase II pilot study investigating the optimal duration of imiquimod 5% cream for the treatment of external genital warts in women.
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An open-label phase II pilot study investigating the optimal duration of imiquimod 5% cream for the treatment of external genital warts in women.

机译:一项开放标签的II期试验研究,研究了5%咪喹莫特乳膏治疗女性外生殖器疣的最佳持续时间。

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摘要

Our objective was to determine the optimal duration of treatment with imiquimod for external genital warts over 4, 8, 12 or 16 weeks. A total of 120 women with a history of genital warts for a median of 3-6 months and prior alternative treatments in 73% were evaluated for total clearance rates. There was no statistically significant difference in complete clearance rates after 16-week follow-up across treatment groups: four weeks (40.0%), eight weeks (48.4%), 12 weeks (39.3%) and 16 weeks (51.6%). Imiquimod was well tolerated, and in those treated for four weeks there was a lower incidence of local skin reactions such as erythema and erosion, and no incidences of pain. These preliminary results suggest that a four-week treatment course of imiquimod applied thrice weekly for women with external genital warts may provide a reasonable approach with comparable efficacy and compliance, and minimal adverse events, drug costs and clinic visits.
机译:我们的目标是确定在4、8、12或16周内使用咪喹莫特治疗外生殖器疣的最佳疗程。评估了总共120名有尖锐湿疣病史,中位数为3-6个月,以前接受过替代治疗的妇女中有73%的妇女的总清除率。各治疗组在随访16周后的完全清除率无统计学差异:4周(40.0%),8周(48.4%),12周(39.3%)和16周(51.6%)。咪喹莫特的耐受性良好,在接受了四周治疗的患者中,局部皮肤反应(如红斑和糜烂)的发生率较低,并且没有疼痛的发生率。这些初步结果表明,对于患有外部尖锐湿疣的妇女,每周三次三次应用咪喹莫特治疗疗程,可以提供一种具有相当疗效和依从性的合理方法,并且不良事件,药物费用和门诊次数最少。

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