Efficacy of an Oral Ageratum Conyzoides Formulation on Increasing Hair Growth and Decreasing Hair Loss in Males and Females: A Randomised Double-Blind Placebo-Controlled Study

P. Clayton, Nathasha Bogoda, Amanda Rao
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Abstract

Background Androgenetic alopecia (AGA) is associated with the enzyme 5a-reductase and prostaglandin D2, both of which are increased in bald areas of the scalp. We previously demonstrated the safety and efficacy of a topical Ageratum conyzoides (A. conyzoides) formulation in improving hair growth and decreasing hair loss. Objective A follow-up 12-week double-blind, randomised clinical trial investigating the efficacy and safety of A. conyzoides extract in an oral formulation, in males and females over 18-years of age. Methods 250 mg of A. conyzoides or a placebo was supplemented daily over a 12-week period to 84 healthy males or females with hair loss. The primary outcome was hair growth assessed by measuring hair density using HairCheck®, and hairline recession. Hair loss was measured by the mean number of hairs lost in a one-minute combing test and hair/tug pull test. Other assessments included Norwood/Hamilton and Ludwig-Savin scales evaluating male and female pattern baldness, respectively. Biochemical and haematological parameters were also assessed, as change from baseline for each group. Results Twelve (12)-week daily supplementation of A. conyzoides resulted in a significant reduction in hairline recession compared to the placebo group. A trend towards significance was observed for hair density between groups, where hair density increased in the A. conyzoides group and decreased in placebo group from their respective baseline values. No significant differences were found in hair loss measures or the Norwood/Hamilton and Ludwig-Savin scales. A significant difference was found in the change from baseline for total prostaglandins between groups at week 12, with a decrease from baseline in the active group and an increase in the placebo group. In males, a significant difference in the change from baseline was seen for type-2 5a-reductase, with a decrease from baseline in the active group and increase in the placebo group. Conclusion These results demonstrate an improvement in hair growth following the 12-week oral supplementation of A. conyzoides extract., with mechanistic convergence.
口服延胡膏制剂促进男性和女性头发生长和减少脱发的疗效:一项随机双盲安慰剂对照研究
背景:雄激素性脱发(AGA)与5a-还原酶和前列腺素D2有关,两者在头皮秃发区域均增加。我们以前证明了安全性和有效性局部鹰嘴藓(a . conyzoides)配方在改善头发生长和减少脱发。目的:通过一项为期12周的随访双盲随机临床试验,研究conyzoides提取物口服制剂在18岁以上男性和女性中的有效性和安全性。方法对84例脱发的健康男性或女性患者进行为期12周的试验,每天补充250 mg的连翘或安慰剂。主要结果是通过使用HairCheck®测量头发密度来评估头发生长和发际线衰退。脱发是通过一分钟梳头测试和头发/拉扯测试中脱发的平均数量来测量的。其他评估包括诺伍德/汉密尔顿量表和路德维希-萨文量表,分别评估男性和女性型秃顶。还评估了每组的生化和血液学参数,作为基线的变化。结果:与安慰剂组相比,每天补充十二(12)周的conyzoides可显著减少发际线衰退。两组之间的毛发密度有显著性的趋势,从各自的基线值来看,棘球菊组的毛发密度增加,而安慰剂组的毛发密度下降。在脱发测量或诺伍德/汉密尔顿和路德维希-萨文量表上没有发现显著差异。在第12周,两组之间的总前列腺素从基线变化有显著差异,活性组从基线下降,安慰剂组从基线上升。在男性中,2型5a还原酶的变化与基线相比有显著差异,活性组较基线降低,安慰剂组较基线升高。结论口服12周后,对毛发生长有改善作用。,具有机械收敛性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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