首页> 外文期刊>Medical Devices: Evidence and Research >Safety and Efficacy of an Oxytocin Gel and an Equivalent Gel but Without Hormonal Ingredients (Vagivital ? Gel) in Postmenopausal Women with Symptoms of Vulvovaginal Atrophy: A Randomized, Double-Blind Controlled Study
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Safety and Efficacy of an Oxytocin Gel and an Equivalent Gel but Without Hormonal Ingredients (Vagivital ? Gel) in Postmenopausal Women with Symptoms of Vulvovaginal Atrophy: A Randomized, Double-Blind Controlled Study

机译:催产素凝胶的安全性和功效,但没有激素成分(阴道般的γ凝胶),患有外销妇女患有外阴萎缩萎缩症状:随机,双盲对照研究

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Purpose: The primary objective was to compare the efficacy of 12 weeks of daily treatment with Aqueous Hypromellose-based vaginal (Vagivital ? ) gel versus Aqueous Hypromellose-based vaginal gel plus 400 IU oxytocin gel in reducing the severity of the most bothersome vulvovaginal atrophy symptoms (MBS: itching, dysuria, bleeding, and pain/discomfort during vaginal sexual activity) observed at baseline. The secondary objectives were to evaluate the other vulvovaginal atrophy symptoms, vaginal pH, superficial squamous cells, and the safety and tolerability of both gels. Patients and Methods: This double-blind, randomized study evaluated the safety and efficacy of subjects randomly assigned to 12 weeks of daily intravaginal oxytocin gel (n=79) or Aqueous Hypromellose-based vaginal gel (n=78). The efficacy evaluation was performed using data from all included subjects who fulfilled entry criteria. Results: Both treatments induced statistically significant reductions in the severity of the MBS from baseline until 4 weeks (Vagivital mean reduction 0.90, p=0.0000; Oxytocin mean reduction 0.82, p=0.0000) and 12 weeks post baseline (Vagivital mean reduction 1.28, p=0.0000; Oxytocin mean reduction 1.16, p=0.0000), but the reduction of MBS severity was not significantly different between the treatment groups at either time point. No serious adverse events were reported in the Aqueous Hypromellose-based vaginal gel group during the treatment period, but one (breast cancer) was reported in the oxytocin gel group (assessed as unlikely related to the study compound). Conclusion: Significant reductions in the severity of the MBS were seen in both the Aqueous Hypromellose-based vaginal gel and the oxytocin gel groups, but with no significant differences in severity reduction seen between the groups. Both gels were safe and well tolerated. Given the benefits of avoiding the use of hormones, Aqueous Hypromellose-based vaginal gel is an attractive first choice in the treatment of postmenopausal women with vulvovaginal atrophy symptoms.
机译:目的:主要目标是将每日治疗12周与含水素水平的阴道(阴道β)的疗效进行比较,而含水氰脲素的阴道凝胶加400IU催产素凝胶在降低最嗜不血萎缩萎缩症状的严重程度(MBS:在基线观察到阴道性活动期间的瘙痒,困困,出血和疼痛/不适。次要目的是评估其他外阴萎缩萎缩症状,阴道pH,肤浅的鳞状细胞,以及两个凝胶的安全性和耐受性。患者和方法:这种双盲,随机研究评估了当前静脉内催产蛋白凝胶(n = 79)的12周或含水氯酰甲酸碱的阴道凝胶(n = 78)的受试者的安全性和有效性。使用来自满足入境标准的所有受试者的数据进行疗效评估。结果:两种治疗致统计学显着降低了基线的MBS的严重程度,直至4周(阴道平均值0.90,P = 0.0000;催产素平均减少0.82,P = 0.0000)和12周后基线(虚拟平均减少1.28,P = 0.0000;催产素平均降低1.16,p = 0.0000),但在任一时点之间的治疗组之间的减少没有显着差异。在治疗期间,在含水氰基水溶液的阴道凝胶基中没有报道任何严重的不良事件,但在催产素凝胶基团中报道了一种(乳腺癌)(评估为不太可能与研究化合物相关)。结论:在基于氰脲素水性的阴道凝胶和催产素凝胶基团中看到MBS的严重程度的显着降低,但在组之间看到的严重程度降低没有显着差异。这两个凝胶都是安全且耐受性的。鉴于避免使用激素的益处,含水素氯脲素的阴道凝胶是一种有吸引力的潜水萎缩萎缩症状的绝经后妇女的首选。

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