首页> 外文期刊>The British Journal of Surgery >Randomized clinical trial of metronidazole ointment versus placebo in perianal Crohn's disease.
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Randomized clinical trial of metronidazole ointment versus placebo in perianal Crohn's disease.

机译:甲硝唑软膏与安慰剂治疗肛周克罗恩病的随机临床试验。

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BACKGROUND: The potential for metronidazole 10 per cent ointment to exert therapeutic benefit in perianal Crohn's disease, while minimizing the adverse effects found with oral metronidazole, was evaluated in a randomized placebo-controlled study. METHODS: Subjects with perianal Crohn's disease were randomized to metronidazole 10 per cent ointment, 0.7 g applied perianally three times daily, or placebo ointment. The Perianal Crohn's Disease Activity Index (PCDAI) was scored at baseline and after 4 weeks of treatment. Perianal pain was assessed on a visual analogue scale. RESULTS: Seventy-four subjects (33 metronidazole, 41 placebo) were evaluated. The mean(s.e.m.) reduction in PCDAI score at 4 weeks was 2.4(0.5) in the metronidazole group and 2.2(0.4) in the placebo group (P = 0.660). More subjects in the metronidazole group than the placebo group showed a reduction in PCDAI score of at least 5 points (10 of 27 versus 4 of 34; P = 0.031). Perianal discharge was reduced significantly in metronidazole-treated subjects (P = 0.012). A greater reduction in perianal pain was seen in the metronidazole group, which approached statistical significance (P = 0.059). No serious adverse events were reported. CONCLUSION: Metronidazole 10 per cent ointment was not effective in the reduction of PDCAI score, but some secondary outcomes showed improvement suggestive of a treatment effect. It is well tolerated, with minimal adverse effects, and has potential as treatment for pain and discharge associated with perianal Crohn's disease. Registration number: NCT00509639 (http://www.clinicaltrials.gov).
机译:背景:在一项随机安慰剂对照研究中,评估了甲硝唑10%软膏在肛周克罗恩病中发挥治疗作用的可能性,同时最大程度降低了口服甲硝唑的不良反应。方法:将患有肛周克罗恩氏病的受试者随机分配到甲硝唑10%软膏,0.7g的肛周软膏中,每日3次,或安慰剂软膏。在基线和治疗4周后对肛周克罗恩病活动指数(PCDAI)进行评分。以视觉模拟量表评估肛周疼痛。结果:对74名受试者(33名甲硝唑,41名安慰剂)进行了评估。甲硝唑组在4周时PCDAI评分的平均下降(s.e.m.)为2.4(0.5),而安慰剂组为2.2(0.4)(P = 0.660)。甲硝唑组的受试者多于安慰剂组,其PCDAI得分降低了至少5分(27分中的10分与34分中的4分; P = 0.031)。在甲硝唑治疗的受试者中,肛周分泌物显着减少(P = 0.012)。在甲硝唑组中,肛周疼痛的减轻更大,接近统计学意义(P = 0.059)。没有严重不良反应的报道。结论:甲硝唑10%软膏不能有效降低PDCAI评分,但一些次要结果显示改善提示治疗效果。它具有良好的耐受性,且副作用极小,并且具有治疗肛周克罗恩氏病相关的疼痛和出院的潜力。注册号:NCT00509639(http://www.clinicaltrials.gov)。

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