A multicentre, randomized, double blind, placebo controlled pilot study to evaluate the efficacy and safety of colloidal Nano silver gel (SilverSol) in the treatment of bacterial vaginosis, vulvovaginal candidiasis and trichomoniasis

Anirudh Mehta, Saurabh Dani, Alaka Godbole
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Abstract

The study evaluated the efficacy and safety of colloidal nano silver gel (SilverSol Vagigel) (A patented technology from American Biotech Labs, USA) in combination with 0.2% lactic acid in the female subjects for the treatment of vaginal infections.This study was a multicenter, randomized, double-blind, placebo-controlled pilot study in which post-menarchal female subjects between 18 and 65 years of age clinically diagnosed with bacterial vaginosis and vulvovaginal candidiasis were enrolled. The participants were randomized to receive treatment with SilverSol Vagigel or placebo (vehicle) gel (both treatments as one 4 gm application inserted into the vagina with an applicator device, once daily at bedtime for internal use and 2 gm gel for local application to the vulva and vagina for external use twice daily for a period of 14 days). The primary endpoint evaluated was the proportion of subjects achieving clinical cure. The secondary endpoint was the proportion of subjects achieving microbiological cure at the end of the study visit. A total of 57 subjects were randomized in the study out of which 38 subjects were randomized in SilverSol Vagigel arm and 19 subjects were randomized in placebo arm. SilverSol Vagigel significantly improved cure rates of vaginal infections compared to placebo. The proportion of subjects achieving clinical cure of vaginal infections was higher i.e., 33 (86.84%) subjects in SilverSol Vagigel arm compared to 07 (41.18%) subjects in Placebo gel arm (p-value: 0.0009). The clinical cure rate with SilverSol Vagigel was 81.82% (P=0.1758) for bacterial vaginosis and 92.59% (P=0.0010) for vulvovaginal candidiasis patients at the end of the study. Overall SilverSol Vagigel treatment resulted in a significantly higher microbial cure of vaginal infections (P=0.0028) compared to placebo, with a microbial cure rate of 100% for bacterial vaginosis (P=0.0330) and 85.19% for vulvovaginal candidiasis (P=0.0097). No adverse events were reported in subjects treated with SilverSol Vagigel.Colloidal Nano Silver Gel (SilverSol Vagigel) was effective and safe in treating bacterial vaginosis and vulvovaginal candidiasis.
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一项多中心、随机、双盲、安慰剂对照试验研究,评估胶体纳米银凝胶(银溶胶)治疗细菌性阴道病、外阴阴道念珠菌病和滴虫病的疗效和安全性
该研究评估了胶体纳米银凝胶(SilverSol Vagigel)(美国美国生物技术实验室的专利技术)联合 0.2% 乳酸治疗女性阴道感染的疗效和安全性。该研究是一项多中心、随机、双盲、安慰剂对照试验研究,研究对象为临床诊断为细菌性阴道病和外阴阴道念珠菌病的 18 至 65 岁女性。受试者被随机分配接受 SilverSol Vagigel 或安慰剂(载体)凝胶的治疗(两种治疗方法都是用涂抹器将 4 克凝胶插入阴道,每天睡前一次,供内服;2 克凝胶供外阴和阴道局部外用,每天两次,为期 14 天)。评估的主要终点是达到临床治愈的受试者比例。次要终点是研究结束时微生物治愈的受试者比例。共有 57 名受试者被随机纳入研究,其中 38 名受试者被随机纳入 SilverSol Vagigel 治疗组,19 名受试者被随机纳入安慰剂治疗组。与安慰剂相比,SilverSol Vagigel 能明显提高阴道感染的治愈率。获得阴道感染临床治愈的受试者比例更高,即 SilverSol Vagigel 组的受试者为 33 人(86.84%),而安慰剂组的受试者为 07 人(41.18%)(P 值:0.0009)。研究结束时,细菌性阴道炎患者使用 SilverSol Vagigel 的临床治愈率为 81.82%(P=0.1758),外阴阴道念珠菌病患者的临床治愈率为 92.59%(P=0.0010)。与安慰剂相比,SilverSol Vagigel 治疗阴道感染的微生物治愈率明显更高(P=0.0028),细菌性阴道病的微生物治愈率为 100%(P=0.0330),外阴阴道念珠菌病的微生物治愈率为 85.19%(P=0.0097)。胶体纳米银凝胶(SilverSol Vagigel)在治疗细菌性阴道病和外阴阴道念珠菌病方面既有效又安全。
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