Thornhill Martin H, Baccaglini Lorena, Theaker Elizabeth, Pemberton Michael N
Department of Oral and Maxillofacial Medicine and Surgery, The University of Sheffield School of Clinical Dentistry, Sheffield, England.
Arch Dermatol. 2007 Apr;143(4):463-70. doi: 10.1001/archderm.143.4.463.
To evaluate pentoxifylline for the treatment of recurrent aphthous stomatitis.
A 60-day, randomized, double-blind, placebo-controlled trial with a 60-day no treatment follow-up.
An oral medicine specialist referral center in Manchester.
Forty-nine volunteers who passed the initial assessment for recurrent aphthous stomatitis entered a pretrial phase in which their eligibility for the trial phase of the study was assessed. Sixteen subjects were deemed ineligible, and 7 failed to attend or withdrew. The remaining 26 subjects were randomized to placebo or treatment. Six subjects withdrew because of adverse effects, and 1 was unavailable for follow-up.
Pentoxifylline (also called oxpentifylline), 400 mg 3 times daily, or matching placebo.
A reduction in the median pain score, ulcer size, number of ulcers, or total number of ulcer episodes.
Patients taking pentoxifylline had less pain and reported smaller and fewer ulcers compared with baseline. Patients taking placebo reported no improvement in these variables. Patients taking pentoxifylline also reported more ulcer-free days than those taking placebo. However, the differences were small and, with the exception of median ulcer size (P = .05), did not reach statistical significance. Adverse effects were common with pentoxifylline, but not significantly different from those experienced by patients taking placebo.
Although pentoxifylline may have some benefit in the treatment of recurrent aphthous stomatitis, the benefit is limited. It may have a role in the treatment of patients unresponsive to other treatments, but cannot yet be recommended as a first-line treatment.
评估己酮可可碱治疗复发性阿弗他口炎的效果。
一项为期60天的随机双盲安慰剂对照试验,随后进行60天的无治疗随访。
曼彻斯特的一家口腔医学专家转诊中心。
49名通过复发性阿弗他口炎初步评估的志愿者进入预试验阶段,在此阶段评估他们参与研究试验阶段的资格。16名受试者被判定不符合资格,7名未参加或退出。其余26名受试者被随机分为安慰剂组或治疗组。6名受试者因不良反应退出,1名无法进行随访。
己酮可可碱(也称为氧甲戊黄嘌呤),每日3次,每次400毫克,或匹配的安慰剂。
中位疼痛评分、溃疡大小、溃疡数量或溃疡发作总数的降低。
与基线相比,服用己酮可可碱的患者疼痛减轻,溃疡更小、数量更少。服用安慰剂的患者在这些变量上没有改善。服用己酮可可碱的患者无溃疡天数也比服用安慰剂的患者多。然而,差异很小,除中位溃疡大小(P = 0.05)外,未达到统计学显著性。己酮可可碱的不良反应很常见,但与服用安慰剂的患者所经历的不良反应无显著差异。
虽然己酮可可碱在治疗复发性阿弗他口炎方面可能有一些益处,但益处有限。它可能在治疗对其他治疗无反应的患者中发挥作用,但目前尚不能推荐作为一线治疗方法。