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首页> 外文期刊>Trials >Oral PSORI-CM01, a Chinese herbal formula, plus topical sequential therapy for moderate-to-severe psoriasis vulgaris: pilot study for a double-blind, randomized, placebo-controlled trial
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Oral PSORI-CM01, a Chinese herbal formula, plus topical sequential therapy for moderate-to-severe psoriasis vulgaris: pilot study for a double-blind, randomized, placebo-controlled trial

机译:口服PSORI-CM01,中草药配方,外用序贯疗法治疗中至重度寻常型牛皮癣:一项双盲,随机,安慰剂对照试验的初步研究

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Background To provide evidence that the Chinese herbal medicine (CHM) PSORI-CM01 combined with Western medicine reduces the relapse rate of psoriasis vulgaris (PV), we plan to conduct a large-scale randomized control trial (RCT). In order to improve and perfect the RCT, this pilot study was designed to determine the feasibility and the potential of a modified protocol for the full-scale RCT. Methods Eligible patients with psoriasis vulgaris (PV) were enrolled into a randomized comparison in which all subjects received topical sequential therapy and PSORI-CM01 or placebo for 12?weeks. The primary outcome measure was the relapse rate. Treatment response was computed from Psoriasis Area and Severity Index (PASI), body surface area (BSA), and Dermatology Life Quality Index (DLQI). The secondary outcome measures included time to relapse, time to onset, rebound rate, PASI score, pruritus scores on the Visual Analog Scale (VAS), BSA, DLQI and SF-36 (short form health survey), and incidence of serious adverse events (SAEs). Results Six of 7 (86?%) subjects reached the PASI-50 in the CHM group compared with nine of 10 (90?%) in the placebo group during the treatment period. Among the subjects who reached PASI-50, one out of six subjects (17?%) relapsed in the CHM group during the treatment period compared with six out of nine patients in the placebo group (67?%). No subjects met the rebound criteria. Changes to baseline in the PASI scores were not significantly different between the two groups ( t =?1.764, P =?0.098). Conclusion Oral PSORI-CM01 combined with topical sequential treatment showed a smaller recurrence rate ( P?=?0.118 ) than placebo combined with the same topical therapy for moderate-to-severe PV in this pilot study. Trial registration Chinese Clinical Trial Registry ( http://?www.?chictr.?org.?cn/?searchproj.?aspx ) ChiCTR-TRC-13003233 ; date of registration: 15 April 2013.
机译:背景为了提供证据证明中草药PSORI-CM01与西药联用可降低寻常型牛皮癣(PV)的复发率,我们计划进行大规模的随机对照试验(RCT)。为了改善和完善RCT,本试验研究旨在确定针对完整RCT的修改协议的可行性和潜力。方法将符合条件的寻常型牛皮癣患者(PV)纳入一项随机对照研究,所有受试者均接受局部序贯治疗和PSORI-CM01或安慰剂治疗12周。主要结局指标是复发率。根据银屑病面积和严重程度指数(PASI),体表面积(BSA)和皮肤病生活质量指数(DLQI)计算治疗反应。次要结局指标包括复发时间,发作时间,反弹率,PASI评分,视觉模拟量表(VAS),BSA,DLQI和SF-36(简短健康状况调查)上的瘙痒评分以及严重不良事件的发生率(SAE)。结果在治疗期间,CHM组7名受试者中有6名(86%)达到了PASI-50,而安慰剂组10名受试者中有9名(90 %%)达到了PASI-50。在达到PASI-50的受试者中,CHM组中有六分之一的受试者(17%)在治疗期间复发,而安慰剂组的九名患者中有六名(67%)。没有受试者达到反弹标准。两组间PASI评分的基线变化无显着差异(t =?1.764,P =?0.098)。结论在本试验研究中,口服PSORI-CM01联合局部序贯治疗显示的复发率(P?=?0.118)低于安慰剂与相同局部治疗相结合的中重度PV复发率。试验注册中国临床试验注册(http://?www。?chictr。?org。?cn /?searchproj。?aspx)ChiCTR-TRC-13003233;注册日期:2013年4月15日。

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