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作 者:储小燕[1] 刘艳[1] 富志良[1] 芦桂青[1] 康莉[1] 毕志刚[1]
机构地区:[1]南京医科大学附属明基医院南京明基医院皮肤科,江苏南京210019
出 处:《中国美容医学》2017年第11期72-74,共3页Chinese Journal of Aesthetic Medicine
摘 要:目的:观察达英35联合2%米诺地尔溶液治疗女性型脱发的临床疗效和安全性。方法:将110例女性型脱发患者随机分成两组。试验组:55例,采用达英35联合2%米诺地尔溶液治疗;对照组:55例,仅外用2%米诺地尔溶液治疗。两组治疗12周后评价疗效及不良反应。结果:治疗12周后,试验组有效率为70.91%,高于对照组的43.64%,两组间差异有统计学意义(P<0.05);睾酮及脱氢表雄酮水平显著低于对照组,差异具有统计学意义(P<0.05)。两组间不良反应发生率比较无显著性差异(P>0.05)。结论:达英35联合2%米诺地尔溶液治疗女性型脱发疗效优于单用2%米诺地尔,且安全性好。Objective To observe the clinical effcacy and safety of Diane-35(Ethinylestradiol and Cyproterone Acetate Tablets) and minoxidil in the treatment of female pattern hair loss. Methods 110 patients with female pattern hair loss were randomly divided into two groups: the experimental group was treated with Diane-35 and minoxidil, while the control group was treated with minoxidil only. The effcacy and side effects was evaluated after treated 12-week treatment. Results After 12 weeks treatment, the total effective rates were 70.91% in the experiment group and 43.64% in the control group (P〈0.05); the sera T and DHEA level of the experiment group Was signifcantly lower than that of the control group (P〈0.05); There were no signifcant difference in side effective rate between two groups. Conclusion It is effective and safe for Diane-35 in combination with minoxidil in the treatment of female pattern hair loss.
分 类 号:R758.71[医药卫生—皮肤病学与性病学]
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