Comparative Examination of the Therapeutic Deficiency of Oral Metronidazole Plus Prangos ferulacea Vaginal Cream Versus Oral Metronidazole Plus Placebo Vaginal Cream in Accelerating Trichomonas Vaginalis Infection Recovery: A Triple-Blind Clinical Trial

Pub Date : 2019-10-06 DOI:10.15296/ijwhr.2020.28
Asieh Azadpour Motlagh, M. Dolatian, F. Mojab, M. Nasiri, Behrouz Ezatpour, N. Sharifi, Narjes Feizollahi, Z. Mahmoodi
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Abstract

Objectives: Trichomonas infection is prevalent in the United States and a metronidazole oral tablet is the medication of choice for treating this infection. Based on various side-effects of oral or vaginal metronidazole and the increase in microbial resistance against chemical antibiotics, the use of herbal medicine with fewer side-effects seems to be essential. Laboratory experiments indicate the strong anti-microbial effects of Prangos ferulacea (PF) medicinal herb. However, no clinical trial has focused on its anti-microbial effects in humans. Thus, the present study aimed to determine the effects of PF vaginal cream on accelerating Trichomonas vaginalis infection (TVI) recovery. Materials and Methods: The present randomized clinical trial was conducted on 80 non-pregnant women visiting the healthcare centers affiliated with Lorestan University of Medical Sciences, Iran, in 2018. Trichomonas infection was diagnosed based on patient complaints, clinical observations, as well as wet mount and stained microscopic tests. The women were randomly divided into two groups of 40 each. One group received oral metronidazole plus PF vaginal cream while the other received oral metronidazole plus placebo vaginal cream for 7 days. Clinical observations, along with wet mount and stained microscopic tests were performed during 7 days following the treatment. Finally, data were analyzed using independent-samples t test, as well as chi-square, Fisher exact, Mann-Whitney U, and McNemar tests at the significance level of P<0.05. Results: Based on the results, the response to treatment with oral metronidazole plus PF vaginal cream was 92.50 based on patient complaints. More precisely, 86.25% was based on clinical criteria (i.e., strawberry cervix, foamy greenish-yellow vaginal discharge, pH ≥4.5, and positive amine test) and 85% was related to the microscopic criteria of wet mount (x40) and polymorphonuclear leukocytes (x100). In addition, the response to treatment with oral metronidazole and placebo vaginal cream was 91.25%, 83.12%, and 80% based on the patient complaint, clinical criteria, and microscopic criteria, respectively. Eventually, the analysis of the patient complaint, clinical criteria, and microscopic criteria in each group revealed a significant difference before and after the treatment (P<0.001) Conclusions: The results of this study showed that the PF herbal vaginal cream can be used for the treatment of TVI as an effective treatment along with oral metronidazole.
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三盲临床研究:口服甲硝唑加阿维果阴道乳膏与口服甲硝唑加安慰剂阴道乳膏加速阴道毛滴虫感染恢复疗效不足的比较研究
目的:滴虫感染在美国很普遍,甲硝唑口服片是治疗这种感染的首选药物。鉴于口服或阴道使用甲硝唑的各种副作用以及微生物对化学抗生素耐药性的增加,使用副作用较少的草药似乎是必要的。实验结果表明,蒲黄具有较强的抑菌作用。然而,尚无临床试验关注其对人体的抗菌作用。因此,本研究旨在确定PF阴道乳膏对加速阴道毛滴虫感染(TVI)恢复的作用。材料与方法:本随机临床试验以2018年在伊朗洛雷斯坦医科大学附属医疗中心就诊的80名非孕妇为研究对象。滴虫感染的诊断依据是患者主诉、临床观察以及湿载和染色镜检。这些女性被随机分为两组,每组40人。一组口服甲硝唑加PF阴道乳膏,另一组口服甲硝唑加安慰剂阴道乳膏,疗程7天。在治疗后7天进行临床观察,以及湿载和染色显微镜检查。最后,采用独立样本t检验,并在P<0.05的显著性水平上采用卡方检验、Fisher精确检验、Mann-Whitney U检验和McNemar检验。结果:口服甲硝唑联合PF阴道乳膏治疗的总有效率为92.50。更准确地说,86.25%是基于临床标准(即草莓子宫颈、泡沫绿黄色阴道分泌物、pH≥4.5、胺试验阳性),85%与显微镜标准湿载(x40)和多形核白细胞(x100)有关。此外,口服甲硝唑和安慰剂阴道乳膏治疗的有效率分别为91.25%、83.12%和80%,分别基于患者主诉、临床标准和显微镜标准。最终,通过对两组患者主诉、临床标准、镜检标准的分析,发现治疗前后差异有统计学意义(P<0.001)。结论:本研究结果表明,PF阴道药膏可与口服甲硝唑联合治疗TVI,是一种有效的治疗方法。
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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