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Protocol of a prospective study for the combination treatment of Shu-Gan-jian-Pi decoction and steroid standard therapy in autoimmune hepatitis patients

机译:疏肝健脾汤联合类固醇标准疗法治疗自身免疫性肝炎的前瞻性研究方案

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Background Prednisone plus azathioprine is considered the mainstay of therapy in the current recommendations for autoimmune hepatitis (AIH). However, it does not provide good benefits for AIH patients because of its serious side effects. Therefore, more and more AIH patients prefer to seek for traditional Chinese medicine (TCM) to manage their symptoms and reduce the side effects of steroids in China. Shu-Gan-Jian-Pi Decoction is a popular used Chinese herbal formula in Guangdong province of China, which has demonstrated the effect of improving efficacy and reducing side effects of corticosteroids in AIH patients. The aim of this study is to evaluate the effects of Shu-Gan-Jian-Pi Decoction combined with steroid in AIH patients. So, this study aims to explore whether the combination treatment of Shu-Gan-Jian-Pi Decoction and steroid standard therapy could improve the clinical management of AIH. Methods A prospective non-randomized study on AIH will be conducted between October 2015 and June 2017 in Guangdong Provincial hospital of Chinese medicine. Eligible AIH patients will be classified as the case group ( n =?66) and the control group ( n =?66) based on the interventions. Patients taking Shu-Gan-Jian-Pi Decoction combined with prednisone and azathioprine will be in the case group and those taking prednisone and azathioprine will be in the control group. The whole study will last 48?weeks, including a 24-week observation period and a 24-week follow-up period. The primary outcome was complete response to therapy, defined as complete biochemical remission at the patient’s last visit of observation period and the absence of predefined steroid-specific side effects throughout treatment. Discussion This trial will evaluate the efficacy and safety of Shu-Gan-Jian-Pi Decoction combined with prednisone and azathioprine on AIH patients. The achievement of this trial will provide evidence-based data for Shu-Gan-Jian-Pi Decoction, which could provide good benefits for AIH patients. Trial registration Chinese Clinical Trial Registry: ChiCTR-OOC-15006155 . Registration date: 28 March 2015
机译:背景泼尼松加硫唑嘌呤被认为是目前针对自身免疫性肝炎(AIH)推荐的治疗手段。但是,由于其严重的副作用,它不能为AIH患者提供良好的益处。因此,在中国,越来越多的AIH患者倾向于寻求中药(TCM)来治疗其症状并减少类固醇的副作用。舒肝健脾汤是中国广东省常用的中草药配方,已证明对改善AIH患者的糖皮质激素疗效和减少副作用。这项研究的目的是评估疏肝健脾汤联合类固醇对AIH患者的疗效。因此,本研究旨在探讨疏肝健脾汤联合类固醇激素标准疗法能否改善AIH的临床管理。方法于2015年10月至2017年6月在广东省中医院进行关于AIH的前瞻性非随机研究。根据干预措施,将符合条件的AIH患者分为病例组(n =?66)和对照组(n =?66)。服用舒肝健脾皮汤联合泼尼松和硫唑嘌呤的患者为病例组,服用泼尼松和硫唑嘌呤的患者为对照组。整个研究将持续48周,包括24周的观察期和24周的随访期。主要结果是对治疗的完全反应,定义为患者在观察期的最后一次就诊时完全生化缓解,并且在整个治疗过程中均未出现预定义的类固醇特异性副作用。讨论本试验将评估舒肝健脾皮汤联合泼尼松和硫唑嘌呤对AIH患者的疗效和安全性。该试验的完成将为疏肝健脾汤提供循证数据,可能为AIH患者带来良好的益处。试验注册中国临床试验注册:ChiCTR-OOC-15006155。报名日期:2015年3月28日

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