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首页> 外文期刊>International Journal of Reproduction, Contraception, Obstetrics and Gynecology >A prospective study to compare the efficacy and safety of tioconazole and clotrimazole vaginal gel in patients suffering from vulvovaginal candidiasis
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A prospective study to compare the efficacy and safety of tioconazole and clotrimazole vaginal gel in patients suffering from vulvovaginal candidiasis

机译:前瞻性研究比较噻康唑和克霉唑阴道凝胶治疗外阴阴道念珠菌病的疗效和安全性

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Background: Vulvo vaginal candidiasis is an extremely common gynaecological condition. While clotrimazole has been the mainstay of treatment of this pathology, newer medications are now available. The study aims to compare the efficacy, compliance and safety of tioconazole single dose intravaginal gel application and clotrimazole vaginal gel for 3 days in patients suffering from vulvovaginal candidiasis. Methods: A prospective, multicentric, open label, randomized, controlled, parallel group clinical trial of 220 women with 110 in each group for the evaluation of the effects of tioconazole vaginal gel in patients suffering from candidial vaginitis. Patients were divided into two groups; Group I received tioconazole vaginal gel as topical single dose therapy administered by the treating doctor and Group II received clotrimazole vaginal gel self-administered by the patient for three days. Response to therapy in both groups was studied and compared. Results: At the end of day 7, mean score of vaginal discharge quantity had a fall of 93.3% and 92.3% in tioconazole and clotrimazole group respectively but difference was statistically insignificant. Microbiological cure rate in both the groups was similar. Reduction of vaginal irritation, vaginal itching, vaginal burning, pain in the vulval area, pain during urination or during sexual intercourse, vaginal erythema, tenderness and swelling were also comparable in both the groups. Conclusions: Tioconazole gel single dose intravaginal application is as effective as clotrimazole gel three day intravaginal application. tioconazole is safe, well accepted and tolerated by the patients and will be useful in the treatment of vulvovaginal candidiasis.
机译:背景:外阴阴道念珠菌病是一种极为常见的妇科疾病。尽管克霉唑一直是这种病理学的治疗手段,但现在已经有更新的药物可供使用。这项研究旨在比较噻康唑单剂量阴道内凝胶剂和克霉唑阴道凝胶剂在外阴念珠菌病患者中使用3天的疗效,依从性和安全性。方法:一项前瞻性,多中心,开放标签,随机,对照,平行分组的临床试验,共220名妇女,每组110名,用于评估噻康唑阴道凝胶剂对念珠菌性阴道炎患者的疗效。患者分为两组。第一组由治疗医生接受噻康唑阴道凝胶作为局部单剂治疗,第二组由患者自行服用克霉唑阴道凝胶三天。研究和比较了两组的治疗反应。结果:在第7天结束时,噻康唑和克霉唑组的白带排出量平均得分分别下降了93.3%和92.3%,但差异无统计学意义。两组的微生物治愈率相似。两组的阴道刺激性,阴道瘙痒,阴道灼热,外阴部疼痛,排尿或性交时疼痛,阴道红斑,压痛和肿胀的减轻也相当。结论:噻康唑凝胶单剂阴道内给药与克霉唑凝胶三天阴道内给药一样有效。噻康唑是安全的,为患者所接受和耐受的药物,可用于治疗外阴阴道念珠菌病。

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